Recommendations are given concerning the terminology of methods of bioanalytical chemistry. With respect to dynamic development particularly in the analysis and investigation of biomacromolecules, terms related to bioanalytical samples, enzymatic methods, immunoanalytical methods, methods used in genomics and nucleic acid analysis, proteomics, metabolomics, glycomics, lipidomics, and biomolecules interaction studies are introduced.
The recommendations contained in this document complete the terminology of bioanalytical chemistry in general and of the analysis of biomacromolecules in particular. The previous IUPAC recommendation, published in 1994, mostly covers analytical terminology related to body fluids, enzymology, and immunology . Elsewhere, selected terms related to bioanalysis are included within the recommendations and reports devoted to the unit “katal” , biotechnology , clinical chemistry , toxicology , , medicinal chemistry , , proteomics , electrochemical biosensors , , and physical organic chemistry . The definitions of some terms have been updated here with respect to new reports and considerations and a number of new terms have been introduced, particularly on the topics of “–omics”, DNA analysis, and studies of the interactions between biomolecules.
These recommendations will become part of a chapter in the revised Orange Book (Compendium of Terminology in Analytical Chemistry, 4th edition).
Bioanalytical chemistry is a branch of science that represents large and dynamic areas of research and practical analytical activities, from human health screening (medical, clinical, food, and pharmaceutical analysis) to forensic analysis and from basic biochemistry studies to special apparatus development.
Bioanalytical chemistry and biochemical analysis often require special methods for sampling and sample preparation and for handling biomolecules, including isolation, purification, separation, and fragmentation. Special attention is paid to apparatus and to techniques with immobilised bioreceptors (biosensors, bioarrays). The methods of analysis and identification of biomacromolecules are radically different from those used to analyse relatively small organic molecules. Most “classical” analytical methods are not suitable for the analysis of biomacromolecules or are suitable only to a limited extent.
There is no complete vocabulary on this topic. With respect to the terminological broadness of the methods used in bioanalysis, the approach taken here is to offer complete and informative definitions specific to bioanalysis without covering definitions utilised generally in branches of analytical chemistry but also widely used in bioanalysis, such as separation methods, mass spectrometry, and others.
Note that “Source: [xx]” indicates a previously published definition with no changes made; “Source: [xx] with minor changes” means that the intent of the existing definition is unchanged but that wording or grammar has been updated; and “Source: Adapted from [xx]” indicates that changes to the definition have been made.
Sub-field of analytical chemistry dealing with analysis of biomolecules.
Bioanalytical chemistry covers the identification (identity, sequence), characterization (properties such as polarity and charge, structure, folding, intermolecular interactions), and quantification and monitoring (stability, dynamics, fragmentation, degradation, metabolism, and others).
Molecule of biological origin.
Most biomolecules are organic compounds present in living organisms. They may also include exogenous molecules modified by metabolism. Some typical biomolecules representing subjects of bioanalytical chemistry are amino acids, peptides, polypeptides, proteins, nucleotides, nucleic acids, carbohydrates, glycoconjugates, lipids, antibodies, haptenes, and receptors, as well as primary and secondary metabolites.
Modern bioanalytical chemistry shifts its attention to the analysis and investigation of biomacromolecules, such as nucleic acids, proteins, polysaccharides, and others.
Macromolecule (including proteins, nucleic acids, and polysaccharides) formed by living organisms.
From a biological standpoint, a biomacromolecule can also be defined as a biomolecule of high relative molecular mass.
Non-natural biomacromolecule-like synthetic molecules, such as poly(lactic acid), and nucleic acid analogues, such as peptide nucleic acid or locked nucleic acid, are also used in bioanalysis.
Substance composed of one type of biomacromolecules.
Modified from the definition given in  in order to avoid confusion between polymer and macromolecule in the fields of proteins, polysaccharides, polynucleotides, and bacterial aliphatic polyesters.
The use of the term “biomacromolecule” is recommended when molecular characteristics are considered.
Substances with a periodic repetition of their biomacromolecular subunits (e.g. polysaccharides such as glycogen, starch and cellulose, polypeptides and polynucleotides).
, term 32 with added example.
Fluid that surrounds the foetus in the amniotic sac.
A specimen is obtained by a technique called amniocentesis, in which a long needle is inserted into the amniotic sac through the abdominal wall, through which fluid is withdrawn.
Fluid that circulates through the heart, arteries, capillaries, and veins.
Circulating blood is a heterogeneous fluid consisting of a clear, slightly yellow liquid (native plasma) and three groups of suspended, formed elements: red blood cells, or erythrocytes (about 99% of the blood cells), white blood cells, or leukocytes, and blood platelets, or thrombocytes. When no anticoagulant is added, normal blood withdrawn from the circulation forms a clot due the polymerization of fibrinogen to fibrin. On standing, the clot retracts, expressing serum which differs from plasma chiefly in that it contains no fibrinogen.
Any cellular element of the blood, including erythrocytes, leucocytes, and platelets.
A blood cell is produced by hematopoiesis and is normally found in blood. In mammals, these fall into three general categories: red blood cells (erythrocytes), white blood cells (leukocytes), and platelets (thrombocytes).
Number of red blood cells and white blood cells per unit volume in a specimen of venous blood.
Red cell phenotypes classified by their antigenic structural characteristics, which are under the control of various allelic genes.
The cell membrane properties that provide the specific antigenicity of the blood groups are called agglutinogens, as they agglutinate or clump in the presence of their specific antibody.
0, A, B
Liquids originating from the bodies of living or dead humans, animals, and other organisms.
They include fluids that are excreted or secreted from the body.
Clear, colourless fluid that fills spaces within and around the central nervous system.
CSF originates from plasma by a biological ultrafiltration process. Specimens are obtained by a lumbar puncture (i.e. a spinal tap).
Blood contained in the vessels of the umbilical cord at the time of birth.
Cord blood contains stem cells.
Yellowish, slightly basic fluid circulating through the lymphatic system.
Lymph is similar to plasma and contains white blood cells.
Blood present in such small amounts that its presence can be ascertained only by chemical analysis or by spectroscopic or microscopic examination; particularly the blood found in stools.
Blood obtained from parts of the body that are located at some distance from the heart.
Blood drawn from the earlobe, fingertip, or heel pad.
Fluid portion of blood in which the blood cells and platelets are suspended.
Plasma is obtained by centrifuging whole blood with anticoagulant addition.
Plasma from which fibrinogen and related coagulation proteins have been removed is called serum.
Sample of blood, serum, or plasma from which all proteins have been removed by chemical or physical denaturation, dialysis, ultrafiltration, or solvent extraction.
Clear, viscous secretion from the parotid, submaxillary, sublingual, and smaller mucous glands in the cavity of the mouth.
Saliva contains many important substances, including electrolytes, mucus, antibacterial compounds and various enzymes.
Watery proteinaceous portion of the blood that remains after clotting. Serum closely resembles plasma except for the absence of some coagulation factors.
Serum contains hydrophilic proteins and electrolytes, antibodies, antigens, hormones, and exogenous substances.
Soft outer covering of vertebrates.
Seminal fluid containing male reproductive cells.
Fluid excreted by the sweat glands in the skin of mammals during perspiration.
Clear salty liquid that is secreted by the lachrymal gland of the eye to lubricate the surface between the eyeball and eyelid and to wash away irritants.
Group of biological cells that perform a specific function.
A cellular organizational level intermediate between cells and complete organs.
Fluid containing metabolic products that is excreted by the kidneys, stored in the bladder, and normally discharged by way of the urethra.
Set of operations for the identification of a component or the measurement of a quantity in analytical chemistry.
Assay is an historical term, now largely obsolete, used as a synonym for the metrological terms examination or measurement. It is still used in compound terms, e.g. immunoassay, bioassay.
 with minor changes.
Set of components (reagents, solutions, and other necessary materials) and procedural instructions needed to perform an assay.
 with minor changes.
Assay in which an effect on an organism, tissue, cell, enzyme, or receptor is compared with the effect of a reference material.
The analyte may be of biological origin (e.g. vitamin, hormone, plant growth factor, antibiotic drug, enzyme).
Discipline encompassing the development and utilisation of computational tools to store, analyse, and interpret biological data.
Among the most important bioinformatics tools are specialised databases with genetic and protein sequences accompanied by related data (biological function, cell localisation, etc.) and including search, alignment, and sorting algorithms or graphical modelling.
biocomponent, at a biosensor
Component of biological origin that translates information from the physicochemical domain into an indication [VIM 4.1] with a defined selectivity [VIM 4.13].
The main purpose of the biological recognition element is to provide a biosensor or other system with a high degree of selectivity for the kind of quantity to be measured.
Typical biological recognition elements include biocatalysts, immune receptors, nucleic acids, and others. Biologically-derived recognition elements, such as oligopeptides, oligosaccharides, and peptide nucleic acids are also of great interest.
A biocatalytic recognition element is based on a biocatalytic reaction. Five types of biocatalyst are commonly used: (a) Enzyme (mono-or multi-enzyme): the most common and well-developed recognition system; (b) whole cells (micro-organisms, such as bacteria, fungi, eukaryotic cells or yeast) or cell organelles or particles (mitochondria, cell walls); and (c) tissue (plant or animal tissue slice). (d) Ribozymes, and (e) DNAzymes.
A biocomplexing or bioaffinity recognition element is based on the binding interaction of the analyte with macromolecules or organised molecular assemblies that have either been isolated from their original biological environment or engineered.
Molecule, specifically related to a particular state of a biological system, used to provide information about an organ function, disease, or other aspect of health.
Biomarkers are traceable substances that are either introduced into an organism or formed in the body.
The molecule signals an event or condition in a biological system or sample and gives a measure of exposure, effect, or susceptibility.
Protein or peptide, nucleic acid, metabolite, hormones, etc.
Adapted from 
Measuring instrument [VIM 3.1] requiring no additional reagents and providing selective qualitative and/or quantitative analytical information using a biological recognition element, which is retained in direct spatial contact with a transduction element (transducer).
The biological recognition system, mediated by isolated enzymes, immunosystems, tissues, organelles, whole cells, or others, translates information from the biochemical domain, usually an analyte concentration, into a chemical or physical (electrical, thermal or optical) output signal with a defined sensitivity.
As a biosensor is a self-contained integrated receptor– transducer device, it should be clearly distinguished from an analytical system that incorporates additional separation steps, such as high performance liquid chromatography (HPLC) or additional hardware and/or sample processing, such as specific reagent introduction, e.g. flow injection analysis (FIA). Thus, a biosensor should be a reagentless analytical device, although the presence of ambient cosubstrates, such as water for hydrolases or oxygen for oxidoreductases, may be required for the analyte determination. HPLC or FIA system may incorporate a biosensor as a detecting device.
It is necessary to distinguish strictly between biosensor (e.g. nucleic acid-based biosensors) and biosensing or bioassay (e.g. nucleic acid sensing).
The variation of a biosensor response depending on the method of preparation and operational conditions is called the biosensor stability. Storage stability and working stability are typically distinguished.
The detection of complementary oligonucleotide sequences by DNA sensors represents selective qualitative information.
Decomposition of organic materials (e.g. starch, sugars, proteins, lignin, hemicelluloses, etc.) with specific enzymes or microbes in which the enzyme converts a high relative molecular mass compound into lower relative molecular mass species.
Enzyme-catalysed hydrolytic degradation of biomolecules.
Investigation of the quantitative relationship between the biological and physicochemical activity of compounds and global parameters representing hydrophobic, electric, steric, and/or other effects using multiple regression correlation.
Hansch analysis is a type of regression analysis used for quantitative structure-activity relationship (QSAR).
Enzyme that catalyses the cleavage of C–O, C–N, and other bonds by a reaction involving water.
See enzymatic decomposition
Procedure or state when the biological recognition element is fixed in a thin layer at the transducer.
Species covalently bound to a biomolecule and used for its detection.
The analytical signal is either a measurable property of the label or is produced by the label.
In an enzyme immunoassay (EIA) the label is an enzyme, in a fluorescence immunoassay (FIA) the label is a fluorescent chemical, and in a radioimmunoassay (RIA) the label is a radionuclide.
Ion, group, or molecule that binds to a specific receptor.
Ion or molecule-like hormone that binds to a biomolecular target to elicit, block, or attenuate a biological response, or to produce a specific analytical signal.
Breaking down of a cell.
Lysis may be caused by physical, (bio)chemical, or biological means.
A fluid containing the contents of lysed cells is called a “lysate”.
Two-dimensional arrangement of a device for analysis of sub-microlitre sample volume.
This screening format is a direct offshoot of genomic microarray technologies and makes use of ultra-low-volume miniaturization provided by nanodispensing technologies.
A collection of molecules spatially addressed on a surface within features that have micrometer dimensions. Planar device (flat plane) used for off-line determination and identification of biocompounds.
As a multiplex lab-on-a-chip, it can be used as an analytical device to measure the mRNA abundance (gene expression) of thousands of genes in one experiment binding the immobilised DNA fragments.
Adapted from 
Molecular structure in or on a cell that specifically recognises and binds to a compound and acts as a physiological signal transducer or as the mediator of an effect.
A receptor can also be immobilised onto a surface used in immunoassays, biosensors, and microchip separation devices.
Time interval after an introduction of the detected analyte at which a signal of the biosensor (the measuring instrument) appears.
Steady-state response time is, by convention, the time necessary to reach 90% of the steady-state response value.
Step response time is the duration between the instant when a signal of the biosensor is subjected to a change (due to a detected analyte) and the instant when a corresponding indication settles within specified limits around its final steady value.
Transient response time is the time necessary for the first derivative of the output signal R to reach its maximum value (dR/dt)max following the addition of an analyte.
Adapted from [VIM 4.23], 
Test of the purity of the sample that will be subjected to detailed biochemical analysis.
Microelectrophoresis belongs to methods used for sample quality testing.
DNA or protein analysis.
The order of neighbouring amino acids in a protein, or of the nucleotides in DNA or RNA.
Adapted from 
Analytical procedures for the determination of the sequence of amino acids in a polypeptide chain (primary structure of a protein) or of nucleotides in DNA or RNA (primary structure of nucleic acid).
See response time (of biosensor)
Part of a biosensor that converts a detected physical or chemical change at the level of the biological recognition element into an observable (usually electronic) signal.
Electrode in voltammetric/amperometric or potentiometric mode, optical fiber, etc.
Adapted from 
See response time (of biosensor)
Phenomenon where the conformation of an enzyme or other protein is altered by combination, at a site other than the substrate-binding site, with a small molecule, referred to as an effector, which results in either increased or decreased activity by the enzyme.
Protein part of an enzyme without the cofactor necessary for catalysis.
The cofactors can be a metal ion (e.g. Cu2+, Cu+, Co2+, Fe3+, Fe2+, Zn2+, Mn2+), an organic molecule (e.g. a coenzyme or prosthetic group), or a combination of both.
enzyme catalytic activity
Property of an enzyme as a biocatalyst, expressed as the rate of the catalysed conversion of a specified chemical reaction produced in a specified assay system.
The SI unit of enzyme catalytic activity, a, is the katal, the enzyme activity that converts one mole of substrate per second under specified reaction conditions. “katal”, kat=1 mol s−1.
The International Unit (U) was defined as the amount of enzyme that catalyses the conversion of one micromole of substrate per minute under the specified conditions of the assay method (1 U=1 μmol min−1≈16.67 nkat). This unit of enzyme catalytic activity was originally proposed by the International Union of Biochemistry in 1964 and is no longer recommended, because the minute is not the SI base unit of time.
Quantities derived from the enzyme activity lead to the following pairs of kind-of-quantity and coherent SI unit:
specific enzyme activity, as=a/m, with the unit katal per kilogram (kat kg−1); molar catalytic activity, am=a/nE, equal to the turnover number, where nE is the amount of enzyme E, with the unit katal per mole of enzyme (kat mol−1).
Catalytic activity divided by the volume of the system.
In clinical chemistry the component is usually an enzyme.
The term catalytic concentration is accepted for use in clinical chemistry.
Use of the term “level” as a synonym for concentration is deprecated.
In describing a quantity, concentration must be clearly distinguished from amount of substance.
Catalytic activity divided by the mass of the system.
The term catalytic content is accepted for use in clinical chemistry.
 page 964
Quotient of the catalytic activity of a particular form of an enzyme, such as isozyme, and the catalytic activity of all the isozymes of the same enzyme in the system.
The term catalytic fraction is accepted for use in clinical chemistry.
The definition also applies to other multiple forms of an enzyme that are not isoenzymes.
Organic molecule that is required by a certain enzyme to carry out catalysis.
This low relative molecular mass and active group of an enzyme is an intermediate carrier of chemically active groups, specific atoms, and/or electrons. A coenzyme binds with its associated protein (apoenzyme) to form the active enzyme (holoenzyme).
Coenzymes may be dissociable or covalently bound. In the latter case they are called prosthetic groups.
The most common is NADH.
Partial or total alteration of the structure of a protein, without change in covalent structure, by the action of certain physical procedures (heating, agitation) or chemical agents (alcohols, tensides, foaming agents).
Denaturation is the result of the disruption of tertiary bonding, which causes the opening of the folded structure of a protein and the loss of characteristic physiologic, enzymatic, or physicochemical properties.
Denaturation can be either reversible or irreversible.
See Lineweaver-Burk plot
Small molecule which increases (activator) or decreases (inhibitor) the activity of an (allosteric) protein by binding to the protein at the regulatory site
The regulatory site is different from the substrate-binding catalytic site.
Macromolecule, usually a protein that functions as a catalyst.
In general, an enzyme catalyses only one reaction type (reaction selectivity) and operates on only one type of substrate (substrate selectivity). Substrate molecules are transformed at the same site (region selectivity); often only one enantiomer of a chiral substrate is transformed.
See Lineweaver-Burk plot
Active enzyme consisting of the apoenzyme and coenzyme (cofactor).
Substance that diminishes the rate of a biochemical reaction.
The process is called inhibition.
See also effector
Related enzymes catalysing the same reaction but having different molecular structure.
Isoenzymes are characterised by different physical, biochemical, or immunological properties.
Plot of the reciprocal of initial velocity of an enzyme-catalysed reaction (ordinate) versus the reciprocal of initial substrate concentration (abscissa).
The plot is used to graphically define the maximum velocity, V, of an enzyme-catalysed reaction and the Michaelis constant for the enzyme.
Eadie-Hofstee plot is an alternative using a linear plot of initial velocity versus the ratio of initial velocity and initial substrate concentration.
Hanes–Woolf plot is another graphical representation of enzyme kinetics which uses a plot of the ratio of the initial substrate concentration [S]0 to the reaction velocity v0 versus [S]0.
See Michaelis-Menten equation
Adapted from .
The relationship between the initial rate (velocity) of an enzyme-catalysed reaction v0 and the initial substrate concentration [S]0 in the form
where V (the limiting rate) and KM (the Michaelis constant) are independent of the initial substrate concentration and constant at a given temperature and a given enzyme concentration. The reaction is then said to display Michaelis-Menten kinetics.
The term ‘hyperbolic kinetics’ is also sometimes used, because a plot of v0 against [S]0 has the form of a rectangular hyperbola through the origin with asymptotes v0=V and [S]0=–KM. This term, and others that imply the use of particular kinds of plot, should be used with care to avoid ambiguity, as they can be misleading if used out of context.
The symbol Vmax and the names “maximum rate” and “maximum velocity” are also in widespread use, although in general and under normal circumstances there is no finite substrate concentration at which v0=V. Hence, there is no maximum in the mathematical sense.
The alternative name Michaelis concentration for KM may also be used and has the advantage of emphasizing that the quantity concerned has the dimension of a concentration and is not, in general, an equilibrium constant. The Michaelis constant is the substrate concentration at which v0=V/2.
See catalytic activity, in enzymology
See catalytic activity, in enzymology
Material introduced with an antigen to augment its immunogenicity.
A substance that helps and enhances the effect of a drug, treatment, or biological system.
Strength of association between a single antibody and a single epitope of antigen.
Affinity of the immunochemical reaction:
is characterised by the affinity (binding, association) constant
The average binding constant reflects a population of antibody molecules (polyclonal antibody).
Immunospecific aggregation of particulate biological matter or synthetic particles.
Immunochemical specific reaction leading to the aggregation of particulate biological matter or synthetic particles.
The biological matter can be bacteria, erythrocytes, or other cells, and the synthetic particles can be polymer beads coated with antigens or antibodies.
Such aggregation is usually primarily dependent on surface reactions mediated by either antigens or antibodies. Physically or chemically, they are attached to the particulate surfaces; agglutination or clumping of the particles follows as a secondary immune reaction.
Type of agglutination in which particulate and soluble antigen compete for soluble antibody.
Typically, it is soluble antigen in the test medium which reacts first with the soluble antibody, inhibiting the agglutination of indicator particles. With viral hemagglutination inhibition assays, host antibodies resulting from a specific infection are the most common forms of agglutination inhibition assays. In this case, viral-specific antibodies block the sites on the virus that agglutinate erythrocytes.
Protein produced by the immune system of an organism in response to exposure to a foreign molecule (antigen).
These proteins are immunoglobulins and bind by means of specific binding sites to a specific antigenic determinant.
An antibody molecule is, by definition, monospecific, but might also be “idiospecific,” “heterospecific,” “polyspecific,” or of “unwanted specificity.” It cannot be “nonspecific”, except in the sense of nonimmunochemical binding.
Substance that stimulates the immune system to produce a set of specific antibodies in a suitable host and will combine with such generated antibodies through its antibody-binding sites (antigenic determinants, epitopes).
Part of the structure of an antigen molecule that is responsible for specific interaction with antibody molecules evoked by the same or a similar antigen.
A serum containing antibodies.
Net affinity of all binding sites of all antibodies in the antiserum under specified physicochemical reaction conditions.
Amount of a ligand that binds to a receptor expressed in operational units.
Operational units are defined in contrast to the quantitative mass units of the affinity constant.
Binding capacity is determined by saturating the receptor and then measuring the amount of complex forming ligand. Parameters like pH and ionic strength influence the capacity value, which will be changed depending on the experimental conditions.
Coating of an immunospecific surface (e.g. serum, tissues, cells, biological macromolecules, biosensor surface) to form an active cover with selectivity or an inert layer.
Blocking is a pre-treatment method with blocking agents (e.g. monovalent Fab fragment, i.e. the antigen-binding fragment of an immunoglobulin molecule; mono or divalent antibodies; organic ligands; metals).
Amount-of-substance ratio of bound to free-labelled analyte.
Protein to which a specific ligand or hapten is conjugated.
Unlabelled protein, introduced into an assay at relatively high concentrations, which distributes in a fractionation process in the same manner as a labelled protein analyte present in very low concentrations.
Protein added to prevent nonspecific interaction of reagents with surfaces, sample components, and each other.
Array of serum proteins (some of which are enzymes) that become sequentially activated after the first member of the series is activated by either antigen-antibody complexes or microbial products.
Material produced by attaching two or more substances together.
Conjugates of antibody with fluorochromes, radioactive isotopes, or enzymes are often used in immunoassays.
Reaction of an antibody with an antigen other than that which elicited the formation due to the presence of related antigenic determinants.
Cross reactivity is due to not ideal selectivity of the antibody.
Conjugate that has an enzyme bound covalently.
Various reporter enzymes, such as horseradish peroxidase (HRP), alkaline phosphatase (AP), and many others can be attached to antibodies. Key substance in ELISA immunoassay.
See antigenic determinant
Low relative molecular mass molecule that contains an antigenic determinant but which is not itself antigenic unless combined with an antigenic carrier.
The carrier may be one that also does not elicit an immune response by itself. It interacts with specific antibody-combining sites of an antibody molecule but is not immunogenic by itself.
Agglutination reactions in which the particles used are erythrocytes.
Hemagglutination may be either direct, in which erythrocyte antigens are reactants, or indirect (passive) for coated antigen or, in the case of reverse (passive) assays, coated antibody. One of the most common uses of hemagglutination is to quantitate the number of hemagglutinating viruses (cf. influenza) or their soluble hemagglutinating surface subunits. It can also be used for blood typing.
Selective reaction of the body to substances that are foreign to it, or that the immune system identifies as foreign, shown by the production of antibodies and antibody-bearing cells, or by a cell-mediated hypersensitivity reaction.
Ligand-binding assay that uses a specific antigen or antibody capable of binding to the analyte.
The antibody can be linked to a radiosotope (radioimmunoassay, RIA), to an enzyme which catalyses an easily monitored reaction (enzyme immunoassay, enzyme-linked immunosorbent assay, ELISA), or to a highly fluorescent compound by which the location of an antigen can be visualised (immunofluorescene, fluorescence immunoassay, chemiluminescent immunoassay).
|Type of immunoassay||Ligand/label||Physical/chemical phenomenon observed|
|radioimmunoassay, RIA, immunoradiometric assay||radioactive nuclide||radioactivity|
|enzyme immunoassay, EIA, and||enzyme like horseradish peroxidase||catalytic activity of a specific enzyme conjugate|
|enzyme-linked immunosorbent assay, ELISA (heterogeneous EIA when antigen or antibody is firmly attached to a solid support)||enzyme like horseradish peroxidase||catalytic activity of a specific enzyme conjugate|
|fluorescence immunoassay||fluorescent compound||fluorescence|
|chemiluminescent immunoassay||chemiluminescent system||chemiluminiscence|
|light-scattering immunoassay||none||changes in turbidity (turbidimetry) or light scattering (nephelometry)|
In general, immunoassays fall into two broad categories: competitive and non-competitive. In a competitive assay, analyte (antigen) in a sample competes with a constant amount of labelled analyte for a limited amount of antibody. For instance, a radioligand assay is a type of radioimmunoassay in which unlabelled and radioactive-labelled molecules of the same analyte compete for a limited number of binding sites on a specific binding protein (an antibody, transport protein, hormone receptor in radioreceptor assay, or any other cell associated receptor or tissue component).
A non-competitive immunoassay involves the capture of all the analyte in the sample by excess antibody, usually immobilised on a solid phase.
Sandwich immunoassay is immunoassay using the chemical or immunochemical binding of analyte to a solid phase and the immunochemical binding of a second (typically labelled) reagent to the analyte. This is one of the most common assays in clinical practice.
Fluorescent excitation transfer immunoassay, fluorescence polarization immunoassay, solid-phase “dipstick” immunoassay, solid-phase microbead fluorescence immunoassay, substrate-labelled fluorescence immunoassay, fluorescence immunoassays using e.g. internal reflectance spectroscopy.
Technique that uses antibodies (or other specific ligands in related techniques) to identify target proteins among a number of unrelated protein species.
The techniques allow the detection of proteins from complex mixtures separated by gel chromatography and then transferred to a membrane. After incubation of the attached product from membrane with labelled antibody, the target proteins become visible.
The extent to which the immunoassay responds only to (all subsets of) a specific analyte and not to other substances of similar structure that are present in the sample.
Study of biochemical and molecular aspects of immunology, especially the nature of antibodies, antigens, and their interactions.
Product of an antigen-antibody reaction that may also contain components of the complement system.
Formation of the immunocomplex is characterised by the binding constant
Substance that elicits a cellular immune response and/or antibody production (cf. antigen).
Antibody which is a large Y-shape protein produced by plasma cells.
As glycoprotein is found in serum or other body fluids and possesses antibody activity.
An individual Ig molecule is built up from two light (L) and two heavy (H) polypeptide chains linked together by disulfide bonds. Igs are divided into five classes based on antigenic and structural differences in the H chains. Ig is used by the immune system to identify and neutralise foreign objects such as bacteria and viruses. It is a protein of the globulin-type structure which is found in serum or in other body fluids that possesses antibody activity.
It denotes also the family of closely related glycoproteins.
Classification of immunoglobulins based on antigenic and structural differences of the heavy peptide chain.
There are five classes: IgG, IgA, IgM, IgD, and IgE.
Immunoglobulin subclass (isotype) represents the subdivision of an immunoglobulin class based on structural and antigenic differences in the heavy peptide chain. Four human IgG subclasses and two IgA subclasses have currently been recognised; IgM subclasses have been postulated; IgD and IgE subclasses are unknown.
Isolation and concentration of an antigen by forming a precipitate with an antibody.
Immunoprecipitation requires that the antibody be coupled to a solid substrate at some point in the procedure.
Kinetic property of the immune reaction caused by an antigen.
Reactivity is defined in  page 1159.
Biosensor where one of the immunointeracting partners (an antibody or an antigen as the analyte) is immobilised on the surface of a physicochemical transducer.
The generated signal either directly reflects the amount of formed immunocomplex or corresponds to the amount of label.
Agglutination in which antigen is first immobilised artificially onto the particulate surfaces, either by physical adsorption or by chemical and/or immunochemical linkers.
Antigen-loaded particles can be used to detect the presence of the corresponding specific agglutinins in sample. Agglutination results by cross-linking of the antigen-bearing particles onto an extensive antigen-antibody lattice (i.e. in detectable agglutination of the particles).
Migration of the sample zone driven by capillary forces in a porous carrier strip.
During migration the dissolved tracer becomes distributed between capture and control zones with immobilised antibodies.
The amount of the label compound in both zones depends on the concentration of the compound in the studied sample.
The most common test of this type is the one for pregnancy.
Arising from a single clone of cells.
In the case of immunoglobulin, ‘monoclonal’ refers to its origin.
Usually, the monoclonal antibody is of a single immunoglobulin class containing only one light chain type of either the K or L variety. It also refers to all antibody molecules having identical physical-chemical characteristics and antibody specificity. Monoclonal antibodies have very restricted structural diversity and they are homogeneous compared with polyclonal antibodies.
Immunoreactivity of an antiserum with its designated antigen
In practice, true monospecificity to naturally occurring antigens does not occur in antisera produced by the immunization of the intact animal. An attempt is made to reduce the level of unwanted specificities below that which will interfere with the intended use of a particular immunochemical test.
Reaction of an antiserum with antihuman IgG.
See also immunochemical specificity
Arising from multiple, different clones.
Polyclonal antibodies (pAbs) are antibodies that are secreted by different B cell lineages within the body. They are a collection of immunoglobulin molecules that react against a specific antigen, each identifying a different epitope.
A typical antiserum obtained from a conventional immunization is polyclonal.
Modification of the indirect agglutination assay, where the particles are coated with antibody.
These antibody-laden particles become probes for detecting specific antigens in the sample material. The presence of the relevant antigen will result in the agglutination of particles.
two-site, noncompetitive immunoassay
Immunoassay using chemical or immunochemical binding of analyte to a solid phase carrying antibody and the immunochemical binding of a second (labelled) reagent to the analyte.
This is one of the most common assays in clinical practice.
Process of producing multiple copies of a DNA sequence by the repeated copying of a DNA segment.
See nucleic acid aptamer
Pair of two nucleobases, consisting of one purine and one pyrimidine base, held together by hydrogen bonds.
In DNA, guanine typically pairs with cytosine and adenine typically pairs with thymine. In RNA, adenine typically pairs with uracil.
See nucleotide sequence
Method for determining the nucleotide sequence.
Computer algorithm that finds regions of local similarity between DNA or protein sequences.
Organised, defined structure of DNA and proteins found in cells. In its nucleotide sequence, it bears the linear array of genes.
Exact copy of biological material.
The biological material can be a DNA segment, whole cell, or complete organism.
Specialised DNA technology for the production of multiple exact copies of a single gene or another segment of DNA.
DNA molecule into which another DNA fragment of appropriate size can be integrated without the loss of its capacity for self-replication.
Artificial DNA that is synthesised in the laboratory from a messenger RNA template.
Nucleotide sequence that can form a double-stranded structure with another DNA sequence by following base-pairing (see base pair) rules.
High-quality, low-error, gap-free DNA sequence of an entire genome of an organism.
Alteration in the DNA chemical structure resulting from interactions with physical or chemical agents occurring in the environment, generated in the organisms as by-products of metabolism, or used as therapeutics.
The main types of DNA damage include the interruption of the sugar-phosphate backbone (strand breaks) or the release of bases due to hydrolysis of N-glycosidic bonds (resulting in abasic sites), inter- and intra-strand crosslinks (such as pyrimidine dimers), and a variety of nucleobase lesions (adducts) resulting from reactions of DNA with a broad range of oxidants, alkylating compounds, and other agents.
Terms “(product of) DNA damage” (lesion, adduct) and “mutation” should not be intermingled. Mutations refer to hereditable changes in DNA sequence—substitutions, deletions, or insertions of (one or more) standard base pair(s) and are not synonyms to “base mismatches”. Importantly, DNA damage and its repair can promote the occurrence of mutations.
Loss of a part (one or more base pairs) of DNA.
Type of pentose sugar that is incorporated in the structure of DNA.
High relative molecular mass linear biological macromolecule composed of nucleotides containing 2-deoxy-D-ribose and linked by phosphodiester bonds. DNA contains the genetic information of organisms.
DNA is a polyanionic macromolecule consisting of chains of nucleotides linked with phosphate bridges (phosphodiester bonds) at the 3′ and 5′ positions of neighbouring sugar (2-deoxy-D-ribose) units (single stranded, ssDNA). Complementary base pairing results in the specific association of two polynucleotide chains that wind around a common helical axis to form a double helix (double stranded DNA, dsDNA). Supercoiled DNA represents a contortion of circular DNA into more complex conformations in which the DNA helices fold around each other. DNA supercoiling is important to assist with DNA packaging within all cells.
DNA contains the genetic information of organisms.
See nucleic acid
Breaking and/or separation of large DNA molecules into smaller pieces (fragments).
DNA fragmentation is usually achieved via cleavage with restriction endonucleases at specific sites or non-specifically by, for example, sonication.
DNA fragmentation is also a consequence of damage to DNA.
Fraction of DNA having fragmented DNA.
Results of sperm DNA damage are generally reported as the percentage of sperm having fragmented DNA, what is called the sperm DNA fragmentation index.
Ratio of longer fragments to shorter DNA.
Integrity index may be clinically usefully used as surrogate for detection of tumours.
DNA strand integrity is measured by quantitative PCR (QPCR) using a real-time system.
Defect in the double stranded DNA structure in which the DNA double helix contains one (or more) non-standard base pairs.
One mismatch is known as a single mismatch. Multiple mismatches are called multi-base mismatches.
Guanine paired with thymine instead of cytosine, or adenine with cytosine instead of thymine.
Identification of individuals by matching characteristics of their genome DNA sequence.
DNA profiles are at a lower resolution than a full genome DNA sequence, but this is adequate for forensic purposes, such as in parental testing and criminal investigations.
Characteristics used include the frequency (or size) of tandem repeats in the genome.
Synthesis of new DNA strands using existing DNA as a template.
Determination of nucleotide sequence (the DNA primary structure).
Next-generation sequencing refers to non-Sanger-based high-throughput DNA sequencing technologies where millions of DNA strands can be sequenced in parallel.
The twisted shape of two complementary DNA strands.
The complementary chains are held together by hydrogen bonds between pairs of the complementary nucleobases. The helical conformation is promoted by several relatively weak interactions, including hydrophobic (stacking) ones between the bases.
The double helix is the most frequent DNA structure formed by two complementary DNA strands. It can also be formed by two complementary RNA strands, one DNA and one RNA strand, as well of any of these with synthetic nucleic acids analogues, such as locked nucleic acid, LNA, or peptide nucleic acid, PNA.
Enzyme that cleaves nucleic acids by hydrolysing phosphodiester bonds between nucleotides within a nucleic acid molecule.
DNA molecule of foreign origin that has been introduced into an organism.
Enzyme that cleaves nucleotides from free ends of a linear nucleic acid molecule.
Molecular unit of heredity of a living organism that encodes a specific feature, usually a protein.
The gene includes, however, regions preceding and following the coding region (leader and trailer) as well as (in eukaryotes) intervening sequences (introns) between individual coding segments (exons).
Functionally, the gene is defined by the cis-trans test that determines whether independent mutations of the same phenotype occur within a single gene or in several genes involved in the same function.
Process for converting a gene’s coded information into biomolecules present and operating in the cell.
Complete set of chromosomal and extrachromosomal genes of an organism, a cell, an organelle or a virus; the complete DNA component of an organism.
Complex and comprehensive study of genome structure and function.
Also, specifically refers to the science of using DNA- and RNA-based technologies to demonstrate alterations in gene expression.
Functional genomics represents a branch of methods to study the sequencing data for description of the gene functions and interactions.
Genetic constitution of an organism as revealed by genetic or molecular analysis.
Incorporation of a nucleotide sequence of DNA into a genome.
See DNA mismatch
Agent that causes a permanent genetic change in a cell.
Alterations in the genomic nucleotide sequence, such as substitutions, insertion, or deletions of single base pairs or of longer DNA stretches.
Technique involving nucleic acids hybridization used to study gene expression at the level of RNA.
The Northern blot approach is opposed to Southern (and other) blots.
Large biomolecule composed of nucleotide subunits.
The major organic matter of the nuclei of a biological cell. It can be hydrolysed into certain pyrimidine or purine bases (usually adenine, cytosine, guanine, thymine, and uracil), D-ribose or 2-deoxy-D-ribose, and phosphoric acid.
Ribonucleic acid and deoxyribonucleic acid.
Single stranded (ss) oligonucleotides (mainly DNA or RNA) originating from in vitro selection, which, starting from random sequence libraries, optimise the nucleic acids for high-affinity binding to a given target.
In vitro selection is an iterative method mainly known as Systematic Evolution of Ligands by EXponential enrichment (SELEX).
Purine or pyrimidine nitrogenous base occurring in DNA or RNA.
Purine and pyrimidine bases of ribo- and deoxyribonucleotides.
a)Uracil is normally found in RNA but not in DNA.
b)Thymine is usually found in DNA but not in RNA.
Product of chemical modification of a nucleobase.
Products of oxidation (e.g. 8-oxoguanine), alkylation (e.g. O6-alkyl guanine), or deamination (e.g. uracil as a product of cytosine deamination).
See also damage to DNA
Compound in which a purine or pyrimidine base is bound via a N-atom to C-1, replacing the hydroxy group of either 2-deoxy-D-ribose or D-ribose, but without any phosphate groups attached to the sugar.
The common nucleosides in biological systems are adenosine, guanosine, cytidine, and uridine, which contain ribose; as well as deoxyadenosine, deoxyguanosine, deoxycytidine, and thymidine, which contain deoxyribose.
Nucleoside in which the primary hydroxy group of either 2-deoxy-D-ribose or of D-ribose is esterified by orthophosphoric acid.
Compounds formally obtained by esterification of the 3- or 5-hydroxy group of nucleosides with phosphoric acid.
Nucleotides are the subunits of nucleic acids.
Nucleotides can be obtained from nucleic acids by hydrolytic cleavage.
Order of nucleotides in a DNA or RNA molecule.
Short nucleic acid typically consisting of up to 50 bases resulting from a linear sequence of nucleotides.
Sequence of DNA or RNA nucleotides, located between the start-code sequence (initiation codon) and the stop-code sequence (termination codon), which is transcribed and translated to generate a protein.
Synthetic DNA mimic, which contains 2-aminoethylglycine linkages instead of the negatively charged phosphodiesteric backbone of oligonucleotides.
The PNA probes are particularly convenient for the detection of single-base mismatches (point mutations, SNPs), because the stability of DNA-PNA duplexes is strongly influenced by a single-base mismatch.
Autonomously replicating extra-chromosomal circular DNA molecule.
Laboratory technique for rapid amplification and pre-determination of regions of double-stranded DNA using DNA polymerase.
See quantitative PCR, real-time PCR
Enzyme that catalyses the synthesis of nucleic acids on pre-existing nucleic acid templates.
Short pre-existing polynucleotide chain attached to a complementary stretch in template DNA to which new deoxyribonucleotides can be added by DNA polymerase.
Single-stranded DNA or RNA molecule used to determine the nucleotide sequence.
Typically, a probe is either immobilised at a surface to capture the complementary target sequence from a sample (capture probe) or labelled, radioactively or immunologically, by fluorescent, electroactive, or other species) to produce a specific signal upon hybridization (signalling or reporter probe).
Nitrogen-containing, double-ring, basic compound that occurs in nucleic acids.
Nitrogen-containing, single-ring, basic compound that occurs in nucleic acids.
Polymerase chain reaction to quantify target nucleotide sequences of interest.
Polymerase chain reaction where data are collected and monitored in real-time as the reaction proceeds.
Digital PCR is a new alternate method to conventional real-time PCR and quantitative PCR for absolute quantification and rare allele detection. Digital PCR works by partitioning a sample of DNA or cDNA into many individual, parallel PCR reactions; some of these reactions contain the target molecule (complementary DNA, positive) while others do not (negative). A single molecule can be amplified a million-fold or more.
DNA molecules joined together using recombinant DNA technology.
Procedure used to join together different DNA segments (sequences).
Recombinant DNA technology can include integration of DNA into the genome of a cell.
Process by which genetic material is broken and joined to other genetic material, which can lead to a rearrangement of genetic sequences.
Process by which DNA polymerase generates two identical copies of DNA from one original DNA molecule.
Different processes of replication have been identified, though cells typically use semi-conservative replication, in which each strand of the original DNA molecule serves as a template for the production of a new strand containing a complementary DNA sequence.
Protein that recognises specific short nucleotide sequences (restriction site) and hydrolyses the DNA backbone at the sequences, generating one (or more) fragments from the DNA molecule.
Variation between individuals in DNA fragment sizes cut by specific restriction enzymes.
Enzyme used to form a complementary DNA sequence (cDNA) from a RNA template.
High relative molecular mass linear biological macromolecule composed of nucleotides containing D-ribose as the sugar and linked by phosphodiester bonds.
RNA molecules play important roles in protein synthesis and other chemical activities of the cell.
Classes of RNA molecules include messenger RNA (mRNA), transfer RNA (tRNA), ribosomal RNA (rRNA), and other types of non-coding RNA with diverse regulatory functions.
See nucleic acid
Single-stranded molecule found in the catalytic core of the ribosome.
Small cellular component capable of performing protein synthesis and composed of specialised ribosomal RNA and protein.
Method for determining nucleotide sequence of DNA based on incorporating chain-terminating dideoxynucleotides.
The method is named after Frederick Sanger (1918–2013, awarded the Nobel Prize in 1958 and 1980).
Method used for determining the order of bases in long DNA using sequencing of DNA broken up randomly into numerous small segments.
See DNA mismatch
Variant of nucleotide sequence of DNA in which the purine or pyrimidine base of a single nucleotide is replaced by another such base.
SNP is the most common type of change in DNA.
SNPs occur normally throughout a human DNA once in every 300 nucleotides on average, which means there are roughly 10 million SNPs in any typical human genome. They can act as biological (diagnostic) markers.
Technique based on DNA hybridization used for the detection of a DNA fragment of specific nucleotide sequence.
Interruption of the sugar-phosphate backbone of a polynucleotide chain.
Multiple consecutive copies of the same nucleotide sequence on a chromosome.
Tandem repeat sequences can be used as markers in physical mapping e.g. by DNA profiling.
Enzyme that directs the replication of telomeres.
Repetitive nucleotide sequences present at the ends of a chromosome that protect the chromosome from deterioration.
In polymer sciences, an oligomer obtained by telomerization is often termed a telomer.
, term 23.
Vector used to clone large DNA fragments.
See cloning vector
Process occurring during gene expression that allows the generation of multiple protein molecules from one gene. It generally involves the processing of mRNA via elimination of introns.
 page 69
Approach to identify proteins and characterise their amino acid sequences or post-translational modifications by sequential combination of proteolysis (enzymatic proteolysis and chemical proteolysis) prior to mass spectrometric analysis of the resulting proteolytic peptides.
In shotgun proteomics, the proteins in a mixture are digested, usually by a specific enzyme, and the resulting peptides are separated by liquid chromatography and identified by tandem mass spectrometry.
See top-down proteomics
Chemical method for C-terminal sequencing of proteins and peptides starting at their C-terminus.
The end of an amino acid chain (protein or polypeptide), terminated by a carboxylic group.
Ion fragmentation technique in mass spectrometry-driven proteomics used to generate peptide fragment ions from proteins in peptide sequencing by tandem mass spectrometry.
Bioinformatics analysis of proteomic mass spectrometric data used in order to identify a protein or its post-translational modification. It results in a list of candidates presented mostly in order of the decreasing statistical significance of the hit.
Mode of two-dimensional gel electrophoresis used to study protein expression regulation by the differential staining of multiple gels representing different states of a proteome, preferably with fluorescent dyes (e.g. Cy3, Cy5, Cy2).
The resulting stained gels are analysed using 2D image analysis.
See expression proteomics
Chemical reduction of protein disulfide bonds.
Reductants, such as tributylphosphine (TBP), 2-sulfanylethan-1-ol (BME), or dithiothreitol (DTT) are used.
 page 101
Method of N-terminal analysis in which the N-terminal amino acid residue is labelled and cleaved from the peptide without affecting other peptide bonds in the peptide chain.
The method is named after Pehr Victor Edman (1916–1977).
Ion fragmentation technique in mass spectrometry-driven proteomics based on the transfer of low energy electrons to the molecules selected for fragmentation.
ETD is particularly effective for analysis of post-translational modification.
Ion fragmentation technique in mass spectrometry-driven proteomics that is a combination of electron-transfer dissociation (ETD) and higher-energy collision dissociation (HCD) in orbitrap instruments.
The dual fragmentation allows generation of rich MS/MS spectra for peptide sequencing and PTM analysis.
Soft ionisation technique in mass spectrometry-driven proteomics.
Electrospray ionisation is optimal for ionising liquid eluates from separation methods, as well as for the direct introduction of liquid samples to fragmentation in MS. Ionisation is made by positive or negative mode, depending on the ability of the molecules to form cations or anions. During the ionisation process, a biomacromolecule obtains a number of charges roughly proportional to its relative molecular mass. Also, non-covalent protein complexes may be ionised with ESI.
Field of study in proteomics that deals with the determination of changes in protein expression and regulation in response to different stimuli, internal or external. It also includes the analysis of post-translational modifications (e.g. phosphorylation, glycosylation, etc.), their identification, and their localisation.
Field of study in proteomics studying protein interactions on different levels: protein-protein interactions (interactomics), the formation of protein complexes, and the interaction of proteins with other biomolecules.
Separation technique used to separate or fractionate proteins and larger peptides according to their relative molecular mass using an electric field in polyacrylamide gel (PAGE).
1D PAGE has two basic modes: a denaturing (or SDS) PAGE to estimate relative molecular masses and a native PAGE to separate proteins as their native structures.
 page 592
Ion fragmentation technique in mass spectrometry-driven proteomics used mostly at orbitrap instruments. It does not have low mass cut-off of collision-induced dissociation (CID) and therefore is used for the tandem mass tag of stable isotope labels.
Separation technique used to separate or fractionate proteins and peptides in a gel (or similar type of media) according to their isoelectric point.
IEF is typically the first dimension of two-dimensional gel electrophoresis.
peptide mass fingerprinting
Protein analysis where an unknown protein is chemically or enzymatically cleaved into peptide fragments whose masses are determined by mass spectrometry. The peptide masses are compared to peptide masses calculated for known proteins in a database and analysed statistically to determine the best match.
Mass spectrometric method used for protein/peptide identification based on protein sequencing.
Using peptide ion fragments, the peptide sequence is read and a list of hit candidates is obtained in combination with database searching.
Non-gel step-wise multi-dimensional technique for separating and identifying individual components of complex protein and peptide mixtures. It combines fractionation of proteolytic peptides in steps on a strong cation exchanger (SAX) using ion exchange chromatography (IEC); each step uses higher elution force. Then, each fraction is separated on reversed phase liquid chromatography and analysed using mass spectrometry.
Chemical method for N-terminal sequencing of proteins and peptides starting at their N-terminus.
See N-terminus and Edman degradation
The end of an amino acid chain (protein or polypeptide), terminating in a free primary amine group.
 page 71
Separation technique used to fractionate proteins and peptides into discrete liquid fractions according to their isoelectric point.
Protein/peptide sequencing approach using overlapping complementary information on a sequence acquired using proteolysis in bottom-up proteomic analysis by at least two different proteolytic approaches.
Amide derived from two or more amino acid molecules (whether of the same or of different molecules) by the formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another with formal loss of water (peptide bond).
The term is usually applied to structures formed from α-amino acids, but it includes those derived from any amino acid.
Usually, when the number is higher than ten, the peptide is expressed using the term polypeptide. An oligopeptide consists of between 2 and 20 amino acids.
Analytical process that derives an amino acid sequence of a peptide from its tandem mass spectrum without the assistance of a sequence database.
It is defined in contrast to protein/peptide identification using a database search. An advantage of de novo sequencing is its applicability to both known and novel peptides from organisms with unsequenced genome.
Product ion which originates in a peptide precursor ion fragmentation process.
Peptide fragment ions are generated in pairs according to the kind of mechanism that dissociates the chemical bonds around the peptide bond.
Mass spectrometric technique that serves to generate peptide fragment ions through the fragmentation of peptide precursor ions via different physicochemical processes in an ion source.
This approach based on the top-down proteomics is an alternative to bottom-up proteomics. The main advantages include the potential for 100% sequence coverage of the protein and improved detection of post-translational modifications.
Peptide ion generated during the ionisation of peptides in an ion source or during tandem mass spectrometry of an intact protein in top-down proteomic analysis, selected for further analysis by means of tandem mass spectrometry.
Once generated, a peptide fragment ion may become a precursor ion for tandem mass spectrometry of higher orders (MSn, n=3).
Study of the set of peptides in an organism, its peptidome.
It uses similar approaches and methods as proteomics.
Set of observable organismal characteristics.
The characteristics can be morphological, developmental, biochemical, or physiological properties, or behaviour.
The diversity of the phenotype is driven by a combination of the gene expression, social, and environmental factors. Proteome plays an important role in the transformation of genotype into phenotype.
 page 1477
Peptide containing ten or more amino acid residues.
 page 1359
Amino acid sequence of the polypeptide chain(s) without regard to spatial arrangement (apart from configuration at the α-carbon atom).
This definition does not include the positions of disulfide bonds and is therefore not identical with ‘covalent structure’.
Naturally occurring or synthetic polypeptide having a relative molecular mass greater than about 10000.
Ensemble of two or more different associated proteins, each with a specific function, linked by non-covalent protein-protein interactions.
Protein complexes are required for most biological processes. Together they form molecular machines that perform biological functions.
Proteins with quaternary structure are not considered as protein complexes.
Anaphase promoting complex.
 page 1572
Set of methods serving to purify the intact protein complex for further analysis.
The methods used may employ single step affinity purification or tandem affinity purification (two affinity purification steps). These approaches include the direct application of an epitope on a bait protein for immunopurification or the genetic insertion of an affinity tag to bait protein, both used to co-purify the prey components of the protein complex.
Collection of protein sequences from several sources, including translations from annotated genetic coding regions, as well as original protein and peptide sequences.
A protein database is fundamental for the determination of protein structure and function via bioinformatics.
 page 109
Physicochemical process by which a polypeptide folds into its characteristic and functional three-dimensional structure from a random coil.
 page 1574
Methodical approach to simplify a complex mixture of proteomic sample.
Target compounds can either be separated into individual protein/peptides or fractionated into groups with similar physicochemical properties (polarity, charge, relative molecular mass, etc.). Different analytical separation methods are deployed to achieve this effect: liquid chromatography, gel electrophoresis, isoelectric focusing, affinity chromatography, etc.
Process which happens during tandem mass spectrometry of intact proteins.
This process is used in top-down proteomics. It generates specific peptide fragment ions from a selected protein precursor ion.
Analytical approach leading to the identity of a protein.
The identity of the protein is given in respect to the proteoform by its primary structure, post-translational modification, or tertiary structure.
 page 14
Supramolecular interacting system, such as a metabolic circuit, intracellular signal transduction, or cell-to-cell communication.
These systems are operated under process control strategies involving integrated feedback control. The input and output of the circuits or modules are coordinated to assure the normal or adaptive function of the cell or organism.
Sequence of the amino acids in the polypeptide chain.
The primary structure of a protein is crucial information for further proteomics analyses.
 page 1579
Series of processes conducted to isolate either the whole proteome or a subset from a biological sample.
Protein purification involves many different methods, such as chromatography, immunopurification, precipitation, etc.
Basic analytical methods used in proteomics to quantitate protein content are gel electrophoresis, immunoanalysis (see Western blotting), densitometry of differential staining and mass spectrometry. Mass spectrometry especially offers many particular techniques based on either stable isotope labelling or label-free approaches.
Absolute quantitation of proteins (AQUA) is performed via measurements on constituent proteolytic peptides using chemically synthesised isotope-labelled peptides as surrogate internal standards for mass spectrometry.
Equipment designed for the automatic determination of amino acid sequences of peptides using a method of N-terminal analysis.
See Edman degradation.
Determination of the primary structure of a protein.
Technique used to visualise proteins separated on electrophoretic slab gels.
Typically, three types of staining are commonly used: silver staining, which is highly sensitive and non-quantitative; Coommassie Brilliant Blue staining, which is less sensitive than silver staining and quantitative; and fluorescent dye staining, which is highly sensitive and quantitative.
All of the different molecular forms in which the protein product of a single gene can be found, including changes due to genetic variations, alternatively spliced RNA transcripts, and post-translational modifications.
Field of biological research in-between proteomics and genomics using proteomic information (mostly derived from mass spectrometry) to improve gene annotations.
Protein cleavage to generate proteolytic peptides for bottom-up proteomic analysis, either enzymatic or chemical.
Both enzymatic and chemical proteolysis may be sequence-specific or unspecific. Proteolysis is specific where cleavage appears at a few specific sequence motives (e.g. proteolysis by trypsin), or unspecific, being connected to wide range of sequence motives (e.g. proteolysis by chymotrypsin).
Exposure of a sample to proteolytic reactions.
Group of enzymes that cleave the polypeptide into shorter oligopeptides (peptides) and amino acids.
 page 1570
Peptide generated via proteolysis.
Complete set of proteins and their modifications in an organismal compartment (organelle, cell, tissue or organism).
The proteome is an analogue of the genome.
Proteome may be viewed as an actual proteome, as a set given by the actual level of protein expression (depending on conditions of growth), or as an overall proteome, a set of all potentially possible proteins expressed according to a given genome.
 page 1586
Complex and comprehensive study of proteomes, particularly proteins, and the way they are expressed, modified, involved in metabolism, as well as of their interactions.
 page 1587
Arrangement of subunits of a protein molecule in space and the ensemble of its intersubunit contacts and interactions, without regard to the internal geometry of the subunits.
A protein molecule not made up of at least potentially separable subunits (not connected by covalent bonds) possesses no quaternary structure. Examples of proteins without quaternary structure are ribonuclease (one chain) and chymotrypsin (three chains).
Type of protein/peptide quantitation, where the relative quantities of one protein in different samples is determined, i.e. the ratio of the content of a protein/peptide in sample 1 to sample 2.
 page 184
Local spatial arrangement of main-chain atoms of a segment of polypeptide chain without regard to the conformation of its side chains or to its relationship with other segments.
Regular sub-structures favoured by specific groups of amino acid sequences; examples include α-helix and β-sheet.
Techniques which serve to quantify protein content by means of mass spectrometry. The principle lies in the introduction of a mass tag to an internal standard protein/peptide containing different stable isotopes than the protein/peptide in the sample. Mass resolved signals originating in the internal standard and the sample are read individually and evaluated.
In the case of a complex sample, the use of multiple reaction monitoring allows for the resolution of multiple overlapping signals.
Field in proteomics which focuses on higher orders of the protein structure, mainly tertiary or quaternary.
Approach in proteomics focused on the selected proteins of a sample.
In a targeted analysis, the mass spectrometer is programmed to analyse a preselected group of proteins. This can be achieved using a technology called selected reaction monitoring (SRM; also referred to as multiple reaction monitoring, MRM), whereby assays are developed on a triple quadrupole instrument to detect fragment-ion signals arising from unique diagnostic peptides representing each of the targeted proteins.
Targeted proteomics achieves the highest sensitivity and throughput for hundreds or thousands of samples in regard to the intended aspect (namely target fragments).
Arrangement of all atoms of a protein molecule or a subunit of a protein molecule in space, without regard to its relationship with neighbouring molecules or subunits.
The tertiary structure represents a three-dimensional fold/organisation of a polypeptide chain, one containing specific arrangements of secondary structures (See secondary structure of a protein).
Approach to identify proteins and characterise their amino acid sequences or post-translational modifications either by direct mass spectrometric analysis of an ionised protein molecule or by sequential combination of protein/peptide fragmentation in the ion source or mass analyser with ion trapping mass spectrometers.
See bottom-up proteomics
Serine protease with highly specific primary endoproteolytic activity that serves to generate proteolytic peptides in bottom-up proteomics analysis.
It may be modified by reductive methylation or glycosylation to increase its thermal stability.
 page 2041
Technique used to separate proteins using isoelectric focusing in a gel. The proteins are then further separated in the second dimension using denaturing PAGE.
2D PAGE greatly enhances the capacity of the separation and facilitates further analysis, such as the difference gel electrophoresis or the mass spectrometric analysis of gel separated proteins.
Immunoanalytical technique for the identification of polypeptides separated using gel electrophoresis. The polypeptide is transferred by blotting to a membrane, where it undergoes specific interaction with primary antibody that is specific to the protein of interest. The peptides are detected as complexes by a label and/or enzymatic reaction, which may be conjugated to the primary antibody directly or via a separate (secondary) antibody.
 page 2101
Sample pretreatment to degrade complex metabolites in the presence of oxygen; a method for amplifying the concentration of native metabolites in solution.
Metabolomic workflow composed of sampling, metabolism quenching, metabolite extraction, metabolite analyses, data analysis, and interpretation.
Complete set of metabolites inside a cell (intracellular metabolites).
Process removing compounds and their metabolites from the body, usually through the kidneys (via urine) or in the feces. Unless excretion is complete, the accumulation of foreign substances can adversely affect normal metabolism.
Complete set of metabolites outside the cell (extracellular environment).
Degradation of the sample compounds in the absence of oxygen; this produces metabolites for intracellular metabolic profile characterization.
Qualitative analysis of the endometabolome.
Profiling and screening the matrix profile with known standards.
In vivo measurements of metabolic fluxes and integration of the results into stoichiometric network models.
Qualitative analysis of the exometabolome.
Glycoside of glucuronic acid.
Glucuronides of xenobiotics (such as drugs, toxic substances, etc.) are formed to excrete them from the organism.
Drug glucuronides and sulfate conjugates are identified in excreted fluids.
All metabolic products of the main compound (e.g. phase 1 and phase 2 metabolites) with the routes of metabolism and the excreted metabolites in body fluids, e.g. in urine or blood.
Set of continuous life-sustaining chemical processes within cells that can be divided into two categories: in catabolism, some substances are broken down to yield energy for vital processes and provide the precursors for biosynthesis, whereas in anabolism, part of this energy and the precursors formed are used to construct new cell components.
Metabolism means the continuously progressive physical and chemical processes involved in the maintenance and reproduction of life in which nutrients are broken down to generate energy and to produce simpler molecules (catabolism), which by themselves may be used to form more complex molecules (anabolism). In the case of heterotrophic organisms, the energy evolving from catabolic processes is made available for use by the organism.
In medicinal chemistry, the term metabolism refers to the biotransformation of xenobiotics and particularly drugs.
Adapted from 
Physical or chemical methodology used for rapidly breaking all biochemical processes in metabolomic samples.
Any chemical compound of the biological system that is not genetically encoded and is a substrate, intermediate, or product of metabolism; is consumed from the external environment; or comes from co-habiting microorganisms, such as gut microflora.
Adapted from 
Unique pattern characterizing the metabolism in a given living phase that does not attempt to identify or quantify all the metabolites.
See fingerprinting and footprinting
Strategy to identify and quantify a particular set of metabolites belonging to a specific metabolic pathway or class of compounds.
Complete quantitative set of organic or inorganic low relative molecular mass compounds (from 50 to 1000) – metabolites – present in the cell or organism and which participate in the metabolic reactions required for growth, maintenance, and normal functioning.
The metabolome forms a large network of metabolic reactions where outputs from one enzymatic chemical reaction are inputs to other chemical reactions.
Complex and comprehensive study of metabolome; identification and quantification of the small molecule metabolic products of a biological system (cell, tissue, organ, biological fluid, or organism) at a specific point in time.
An essential part of systems biology in addition to genomics, transcriptomics, proteomics, interactomics, and fluxomics.
Measurement of the dynamic multiparametric metabolic response of a living system to pathophysiological stimuli or genetic modification.
This term is sometime misapplied to refer to the whole of “metabolomics”.
Metabolites directly involved in the normal life processes of each cell.
alcohols, amino acids, monosaccharides, nucleotides, organic acids.
Metabolites not required for the survival of the corresponding organism, but which have other important functions.
antibiotics, pigments, attractants, flavours, drugs, biomarkers.
Activated form of monosaccharide linked to a nucleotide to be available in a high-energy state for glycosyl transfer.
The non-sugar compound remaining after the replacement of the glycosyl group from a glycoside by a hydrogen atom. Non-carbohydrate part of a glycoconjugate or a glycoside.
The alternative spelling aglycone is discouraged because it suggests a ketonic structure.
Monosaccharide with an aldehydic carbonyl or potential aldehydic carbonyl group.
The term potential aldehydic carbonyl group refers to the hemiacetal group arising from ring closure.
glycosidic hydroxy group
Hydroxy(l) group that originates from the aldehydic or ketonic group of a monosaccharide after ring closure.
A functional group in one of two stereoisomers of a cyclic saccharide that differs only in its configuration at the hemiacetal or hemiketal carbon, which is also called the anomeric carbon. An anomer is a special type of epimer.
See hemiacetal and hemiketal
Monosaccharides, oligosaccharides and polysaccharides, as well as substances derived from monosaccharides by reduction of the carbonyl group (alditols), by oxidation, including the oxidation of one or more terminal groups to carboxylic acids, or by replacement of one or more hydroxy groups by a hydrogen atom, an amino group, a thiol group, or by similar heteroatomic groups. This term also includes derivatives of these compounds.
The term carbohydrate was applied originally to monosaccharides, in recognition of the fact that their empirical composition can be expressed as Cm(H2O)n. However, the term is now used generically in a wider sense.
See glycan-binding protein
Field of glycoproteomics that studies that the changes in the structures and expression levels of glycoproteins under different conditions.
Field of proteoglycomics that studies the changes in the structures and expression levels of proteoglycans under different conditions.
The term includes oligosaccharides and polysaccharides, either free or bound to other chemical entities (glycoconjugates).
Glycans attached to a surface of a microarray.
Glycan microarrays are used for the characterization of lectins and other glycan-binding proteins via specific interactions with labelled glycan-binding proteins.
Specific lectin–glycan interactions are also used for the characterization of glycans in the opposite set-up (see lectin microarray, glycan profiling).
Determination of the diversity of glycan structures expressed on glycoconjugates or cells.
See lectin microarray
Protein that recognises and binds to specific glycans and mediates their biological function.
Compound in which glycan is covalently bound to other chemical species.
The glycan part of a glycoconjugate is called glycone. The non-sugar part is called aglycon.
Specific form of a glycoprotein containing a distinct glycan structure per glycosylation site.
Natural glycoprotein consists of a population of glycoforms resulting from variable glycan structure and/or glycan attachment site occupancy.
Gene encoding an enzyme or other functional protein for glycan synthesis.
The term should not be confused with glycogen (an energy-storage glucose polysacharide in animals and fungi).
Proteins for glycan synthesis include glycosyltransferases, sugar-nucleotide synthases, sugar-nucleotide transporters, and sulfotransferases (see glycosylation, activated nucleotide sugars).
Compound containing a glycan covalently linked to a lipid aglycon.
The term “lipid” comprises several types of compounds. Therefore, different classes of glycolipides are described. For example, typical glycolipids in higher organisms are glycosphingolipids.
Complete set of glycans and glycoconjugates produced by a species, tissue, or cell in a specified time, space, and environment.
Glycome is an analogue of the terms genome, proteome, and transcriptome.
The terms, as for example “sialome”, are sometimes used for the specific subclasses of the glycome.
Complex and comprehensive study of the glycome.
An analogue of the terms genomics or proteomics. The terms, as for example “fucanomics” or “galactanomics”, are sometimes used for the specialised fields of glycomics.
Carbohydrate part of a glycoconjugate or a glycoside.
Protein with one or more covalently bound glycans.
Comprehensive analysis of glycoproteins.
Glycoproteomics studies the glycosylated subset of the proteome, including sites of glycosylation and glycan structures.
Long, linear, highly-charged polysaccharide composed of disaccharide repeating units, each containing hexose or hexuronic acid and N-acetylated or substitution-free hexosamine.
GAG could be a free complex polysaccharide or be covalently linked to a protein core.
Enzyme that catalyses the hydrolysis of glycosidic linkages.
Endoglycosidase hydrolyses internal glycosidic linkages, while exoglycosidase removes terminal monosaccharide from the non-reducing end of a glycoside.
Mixed acetal formally arising by the elimination of water between the hemiacetal or hemiketal hydroxy group of a sugar and a hydroxy group of a second compound. Glycan containing at least one glycosidic linkage to another glycan or an aglycon.
The bond between the two components is called a glycosidic bond.
Linkage of a monosaccharide to another residue via the anomeric hydroxy(l) group.
See anomeric hydroxy(l) group
Monosaccharide ring without the anomeric oxygen.
Adapted from 
Covalent attachment of a saccharide to a protein, lipid, polynucleotide, saccharide, or other organic compound, generally catalysed by enzymes glycosyltransferases.
Enzyme that catalyses the transfer of a saccharide from a nucleotide di(mono)phosphate-activated sugar to an acceptor molecule.
See activated nucleotide sugars, glycosylation
Compound having the general formula RCH(OH)(OR′) (R′≠H).
A hemiacetal results from the nucleophilic addition of a hydroxy group to a carbonyl functionality of an aldehyde, as in ring closure of an aldose.
See anomeric hydroxy(l) group, hemiketal
Compound having the general formula R2C(OH)OR′ (R′ ≠ H).
A hemiketal results from the nucleophilic addition of a hydroxy group to a carbonyl functionality of a ketone, as in ring closure of a ketose.
Monosaccharide with a ketonic carbonyl or a potential ketonic carbonyl group.
Saccharide binding protein of non-immune origin.
Some lectins participate in immune system processes, but they are not products of primary immune response. Lectins also do not display catalytic activity towards their ligands; the binding of carbohydrate is reversible and highly specific.
Adapted from 
Lectins with distinct saccharide-binding specificity arranged on a microarray platform.
Lectin microarray is used for the characterization of glycans (see: glycan profiling) via specific interactions with labelled glycans.
The specific lectin–glycan interactions are also used for the characterization of lectins in the opposite set-up (see: glycan microarray).
Polyhydroxy aldehyde H-[CHOH]n-CHO or polyhydroxy ketone H-[CHOH]n-CO-[CHOH]m-H, with at least with three or more carbon atoms, respectively.
The generic term monosaccharide (as opposed to oligosaccharide or polysaccharide) denotes a single unit without glycosidic connection to other such units.
Most monosaccharides exist as cyclic hemiacetals or hemiketals.
Aldoses, dialdoses, aldoketoses, ketoses, diketoses, as well as deoxy sugars and amino sugars, and their derivatives, provided that the compound has a (potential) carbonyl group.
See activated nucleotide sugar
Compound in which monosaccharide units are joined by glycosidic linkages.
Oligosaccharides are called disaccharides, trisaccharides, tetrasaccharides, pentasaccharides, etc., according to their number of units.
Adapted from 
Biomacromolecule consisting of a large number of monosaccharide (glycose) residues joined to each other by glycosidic linkages.
Compound consisting of a protein core to which one or more glycosaminoglycan chains are covalently attached.
Systematic study of the structure, expression, and function of proteoglycans.
The generic term applied to monosaccharides, oligosaccharides, and polysaccharides.
The term frequently applied to monosaccharides and lower oligosaccharides.
Treatment with alkaline solution (e.g. hydrazine, KOH, NaOH) useful for the cleavage of fatty acids.
The resulting (partially or fully) O-deacylated and (fully) N-deacylated products enable the determination of the fatty acid substitution positions by mass spectrometry.
Adapted from 
Intermediate structural region between the O-polysaccharide and lipid A moiety of lipopolysaccharides (LPS).
Aliphatic rnonocarboxylic acids derived from or contained in esterified form in an animal or vegetable fat, oil, or wax.
Fatty acids are building blocks of the majority of complex cellular lipids, such as phospholipids, sphingolipids, triacylglycerols, and sterylesters.
Adapted from 
Diverse group of lipid molecules synthesised by chain elongation of an acetyl-CoA primer with malonyl-CoA (or methylmalonyl-CoA) groups.
The fatty acyl category is further divided into multiple subclasses, including fatty acids and conjugates, icosanoid, fatty alcohols and esters, glycans, and others.
Palmitic acid, oleic acid, octanedioic acid, prostaglandin A1, leukotriene B4.
Adapted from 
Esters, ethers, and other O-derivatives of glycerol with alkyls or alkenyls, including mono-, di-, and tri-substituted glycerols.
1-dodecanoyl-sn-glycerol (monoacylglycerol), 1-dodecanoyl-2-hexadecanoyl-3-octadecanoyl-sn-glycerol (triacylglycerol).
Lipids with glycerol backbone esterified with one or two fatty acids in position C-1 and/or C-2 and with phosphoric acid at position C-3. The phosphate group is usually esterified with an alcohol (choline, ethanolamine, serine, inositol, glycerol) to form the “lipid head group”.
GP are ubiquitous in nature and are key components of the membrane lipid bilayers of cells.
phosphatidyl choline, phosphatidyl ethanolamine, plasmalogens.
Unsaturated C20fatty acids and skeletally related compounds. Biologically active lipid mediators, including prostaglandins, thromboxanes, leukotrienes, and other oxygenated derivatives, which are produced primarily by three classes of enzymes, cyclooxygenases (COX-1 and COX-2), lipoxygenases (LOX) and cytochrome P450 mono-oxygenases.
The spelling icosanoids is preferred over the spelling eicosanoids for consistency with icosanoic acid.
Glycolipid component of lipopolysaccharides (LPSs) that is integrated into the bacterial cell wall and is responsible for the beneficial (immunostimulatory) or toxic (immunopathological) effects of the molecule.
The archetypical (Enterobacteriaceae) structure of lipid A consists of a β-1,6-linked d-glucosamine (GlcN) or 2,3-diamino-2,3-dideoxy-d-glucose (GlcN3N) disaccharide (or a mixture of them), which is acylated by varying numbers (usually four to seven) of ester- and amide-linked acyl groups (often termed primary and secondary fatty acids). Phosphate groups and other glycosyl substituents may be linked at the C-1 and C-4′ positions. Lipid A is linked to the core oligosaccharide at the C-6′ position of the distal sugar unit of lipid A.
Round-shaped intracellular inclusions consisting of hydrophobic cores (mainly triacylglycerols, sterol esters, occasionally free fatty acids or squalene) covered by a phospholipid monolayer containing a specific set of proteins.
Originally considered as lipid storage compartments, lipid droplets are currently recognised as organelles with high metabolic activity. The defective formation and/or function of lipid droplets is involved in various pathogenic conditions, such as obesity, cardiovascular diseases, type 2 diabetes, or metabolic syndrome.
Isolation of lipids in their native state from samples of different origin.
Usually based on the use of organic solvents (methanol, chloroform) to facilitate lipid partitioning between aqueous and organic phases.
Lipidomics technique conferring unbiased information about total lipids within a particular cell type, tissue, or body fluid.
Changes in the lipid molecules composition after completion of their biosynthesis.
In glycerophospholipids, remodelling includes changes in the composition of fatty acids (for example by acyl chain exchange catalysed by transacylases) or the introduction of unsaturated double bonds (catalysed by desaturases), or by the synthesis of new lipid species or degradation of existing ones. In phosphoinositides, it can involve phosphorylation/dephosphorylation processes.
Lipid remodelling is important for the adaptation of biological membranes to changing environmental conditions and physiological demands.
Complete set of lipid species and their metabolites present within a particular cell type, tissue, or body fluid.
It is estimated that lipidome of a eukaryotic cell may contain over 100000 individual molecular species of various lipids.
Systematic and comprehensive study aimed at the identification, profiling, and quantification of lipidome.
In a broader context, lipidomics includes system-level analysis of subcellular localization and the biological activities of individual lipids.
Lipidomics is a lipid-targeted metabolomics approach aimed at a comprehensive analysis of lipids in biological systems.
Small, biologically active molecules of variable structure, commonly defined by their solubility in non-polar solvents. Hydrophobic or amphipathic small molecules that may originate, entirely or in part, by the carbanion-based condensations of thioesters (fatty acyls, glycerolipids, glycerophospholipids, sphingolipids, saccharolipids, and polyketides) and/or by carbocation-based condensations of isoprene units (prenol lipids and sterol lipids).
Lipopolysaccharides produced by specific wild-type bacteria that give a smooth-colony appearance when cultured on agar plates.
LOSs are composed of lipid A and a saccharide moiety, limited to an oligosaccharide core only.
The lack of O-polysaccharide chains in LOS structures is an inherent property of bacteria.
Principal structural component of the outer leaflet of the outer membrane of gram-negative bacteria and cyanobacteria. It forms a tight permeability barrier that prevents the passage of cell-damaging agents (detergents, bile salts, hydrophobic antibiotics) into the cell.
The chemical structure of an LPS molecule is divided into three covalently linked segments: the O-polysaccharide, the core oligosaccharide (featuring an inner and outer region), and the lipid A moiety.
The biological activity of LPS, LOS, or lipid A molecules as endotoxins in terms of host-mediated responses to LPSs or related compounds is called endotoxic activity (endotoxicity).
Beyond this general structure, there are variations in all parts of LPS, depending on the bacterial strain from which the LPS originate.
Study of the structure-activity relationship of bacterial lipopolysaccharides.
Planar structure spontaneously formed by amphipathic lipids in a polar (aqueous) environment.
Formation of a lipid bilayer is driven by the interaction of the polar heads of lipids with water molecules while minimizing the exposure of the hydrophobic parts of lipids to water. Lipid bilayers represent the basic structure of biological membranes.
Dynamic, nanometre-sized, highly ordered, membrane domains enriched in sterols and sphingolipids. They contain specific sets of membrane proteins that are sorted into rafts by their specific physical properties and specific lipid-protein interactions.
In functional terms, membrane rafts represent highly specialised membrane domains involved in various cellular processes, such as transmembrane transport, membrane trafficking, cell signalling, or virus assembly.
Specific structure of lipid molecules (glycerophospholipids) in aqueous environments and membranes as a function of the ratio between the cross-sections of their polar heads and hydrophobic tails.
Lipids’ ability to self-assemble in dynamic macrostructures in an aqueous medium is driven by the amphiphilic nature of lipid molecules, which tend to aggregate so that the hydrophobic (tails) and the hydrophilic (heads) parts of the lipid are well separated and the area of the dividing surface is held by the hydrophobic effect.
The shape of a membrane lipid depends on the relative size of its polar headgroup and apolar tails. In cases in which the headgroup and lipid backbone have similar cross-sectional areas, the molecule has a cylindrical shape (phosphatidylcholine and phosphatidylserine). Lipids with a small headgroup, such as phosphatidylethanolamine, are conical shaped. By contrast, when the hydrophobic part occupies a relatively smaller surface area, the molecule has the shape of an inverted cone (lysophosphatidylcholine and, to some extent, sphingomyelin).
Part of lipopolysaccharide that consists of a polysaccharide chain extending outwards from the bacterial cell surface.
Assemblies of lipids and proteins in blood plasma transporting lipids between tissues.
They are structurally very similar to intracellular lipid droplets. They are classified according to their size and buoyant density into five types with different functions: chylomicrons, very low density lipoproteins (VLDL), intermediate lipoproteins (IDL), low density lipoproteins (LDL), and high density lipoproteins (HDL).
Heterogeneous group of compounds assembled from simple acyl building blocks made up of polyethers, polyenes, polyphenols, macrolides, and enediynes.
Many polyketides are cyclic molecules whose backbones are often further modified by glycosylation, methylation, hydroxylation, oxidation, and/or other processes.
erythromycin, nystatin, tetracyclines.
Fatty acids with more than one double bond.
The double bonds usually have cis (Z) configuration and are methylene-interrupted.
linoleic and arachidonic acids.
Lipids containing a linear chain of isoprenoid groups.
Prenol lipids are synthesised from the five-carbon precursors isopentenyl diphosphate and dimethylallyl diphosphate. Both precursors are produced mainly via the mevalonic acid pathway.
vitamin A, vitamin E, vitamin K, ubiquinone, β-carotene.
Proteins with covalently linked lipids, e.g. fatty acid or glycophosphatidylinositol (GPI).
The term ‘lipoprotein’ is also occasionally used to describe such compounds, but to avoid confusion this might be better reserved for the non-covalently linked lipid-protein complexes of the type found in plasma (plasma lipoproteins).
Biomolecules where fatty acids are directly bound to a saccharide backbone, thus forming structures similar to glycerolipids or glycerophospholipids, with saccharide substituting for the glycerol.
lipid X (diacylaminosugar), Kdo2LipidA (acylaminosugar glycan).
Methodological approach based on the direct analysis of the total lipid extracts from cells or tissues without an online chromatographic separation.
Lipid molecules involved in intracellular signalling and the regulation of cell death, immune response, or inflammation.
Signalling lipids include diacylglycerol, phosphatidic acid, phosphatidylinositol-4,5-bisphosphate (the source of polyphosphorylated inositols), arachidonic acid-derived mediators (icosanoids, prostaglandins and leukotrienes), sphingolipid-derived mediators (ceramides, sphingosine, sphingosine-1-phosphate), or cholesterol-derived steroid hormones (androgens, estrogens, progestogens, mineralocorticoids, glucocorticoids).
Broadly defined term referring to any lipid messenger that binds a protein target, such as a receptor, kinase or phosphatase, which in turn mediates the effects of these lipids on specific cellular responses.
A complex family of lipids that contain a sphingoid base backbone and a fatty acyl chain.
Together with glycerophospholipids and sterols, sphingolipids are the major lipid components of cellular membranes.
Subclasses are represented by ceramides, gangliosides, sphingosines, sphingomyelines.
Structural derivatives of tetracyclic alcohols with a hydroxyl group in the position C-3 and an aliphatic side chain in the position C-17.
This category primarily comprises sterols: polycyclic compounds of isoprenoid origin and their various derivatives, including steroids, bile acids, and sterol esters. Sterols, along with glycerophospholipids and sphingolipids, are important constituents of cellular membranes. In addition, sterol lipids act as hormones (steroids) or fat emulsifiers (bile acids).
Subclasses are represented by cholesterol, ergosterol, taurocholic acid, glucuronides.
Lipids (mainly glycerophospholipids, sterols and sphingolipids) involved in the formation of biological membranes.
Analytical technique focusing on the quantification of specific lipids of interest.
A number indicating the proportion of double bonds in fatty acids moieties of phospholipids.
UI is indicative of membrane physical properties (e.g. fluidity, curvature, or flexibility).
Specifically-designed single-stranded nucleic acid with a defined (known) nucleotide sequence immobilised on a surface.
Capture probes are utilised as a recognition element to test the nucleotide sequence of target DNA or RNA in the sample solution by using DNA or RNA hybridization.
An analogous principle, based on immobilised nucleic acid probes, has been applied in studies of the interactions of nucleic acids with proteins or other targets. See also nucleic acid aptamers.
Nucleic acids: ssDNA (alternatively, RNA or a synthetic nucleic acid analogue, such as LNA or PNA). Surfaces: microarray, magnetic, or other micro/nanoparticle, a transducer of the biosensor.
Method for studying DNA–protein and/or protein–protein interactions in the context of chromatin, suitable for the identification of binding sites of proteins in genome DNA, etc. This method combines chemical cross-linking, the isolation of specific protein conjugates by immunoprecipitation, and PCR amplification of co-precipitated DNA.
Formation of a covalent bridge between two biomacromolecules or between two segments of the same biomacromolecule using reactive substances (e.g. formaldehyde, bifunctional aldehydes such as glutaraldehyde, or cisplatin) or photochemical processes.
Cross-linking is used to study protein oligomerization, as well as protein–protein and nucleic acid–protein interactions
See chromatin immunoprecipitation
Cytogenetic technique used to detect and localise the presence or absence of specific DNA sequences on chromosomes. It uses fluorescent probes that only bind to those parts of the chromosome with which they show a high degree of sequence complementarity.
FISH is often used for finding specific features in DNA for use in genetic counselling, medicine, and species identification. FISH can also be used to detect and localise specific RNA targets (mRNA, lncRNA and miRNA) in cells, circulating tumour cells, and tissue samples. In this context, it can help define the spatial-temporal patterns of gene expression within cells and tissues.
Process in which molecules are bound within a minor or major groove of the DNA double helix.
Process of forming a double-stranded molecule from two strands of DNA, RNA or synthetic nucleic acids analogues (e.g. PNA, LNA) with complementary sequence.
DNA hybridization as a chemical interaction based on the ability of ssDNA to form a DNA double helix (dsDNA) with a counterpart molecule consisting of a complementary nucleotide sequence.
Assay with specifically designed single-stranded DNA probe with a defined (known) nucleotide sequence usually immobilised on a surface (in such a case, the nucleic acid probe is called the capture probe).
The probe is used as a recognition element to test for the nucleotide sequence within the target DNA in the sample solution. If target DNA contains a sequence complementary to the probe, a hybrid dsDNA is formed.
Virtual map depicting protein–protein interactions.
The interactome is the most visible outcome of functional proteomics.
Adapted from 
Complex and comprehensive study of the interactions between various proteins and between protein and other molecules within a cell, such as nucleic acids and metabolites, as well as the consequences of these interactions.
Thermodynamically favourable, reversible inclusion of a molecule (or group) between two other molecules (or groups).
An insertion of guest molecules between the stacked base pairs of the DNA double helix (double stranded DNA) structure. It typically occurs with compounds of a planar structure with 3–4 condensed aromatic rings. To accommodate an intercalating molecule, the DNA double helix must lengthen and unwind slightly.
Interactions between (parts of) two biomolecule chains (e.g. base pairing in DNA double helix, or the interactions between two polypeptide chains, or between a DNA and a protein molecule).
Interactions between (neighbouring or distant) segments within the same biomolecule chain (e.g. base pairing in hairpin or monomolecular tetraplex structures of DNA or RNA, the interactions stabilizing the secondary or tertiary structures of proteins, etc.).
Interactions between biomolecules or within a biomolecule (e.g. hydrogen bonds, electrostatic interactions, and van der Waals forces) taking part in the stabilization of proper biomolecule structure and intermolecular interactions.
Binding of a protein to DNA independent of the nucleotide sequence or the conformation of the DNA, often with a strong contribution of electrostatic interaction between the negatively charged sugar-phosphate backbone of the DNA and basic amino acid residues of the protein.
Formation of specific or non-specific complexes between DNA or RNA and proteins, mediated and stabilised by a network of non-covalent interactions.
Nucleic acid–protein interactions are critical for basic cellular functions such as replication, transcription, translation, recombination, DNA repair etc. as well as for fine regulation of them. Proteins may bind more tightly to specific sequences in the nucleic acid or non-specifically, in which case their affinity is independent of sequence.
Association of one protein with one or more other proteins to form either homo- or heteromeric proteins or protein complexes.
Such associations are common in biological systems and are responsible for the regulation of numerous cellular functions in addition to the mediation of disease morphology, where aberrant interactions play a significant role.
Approach used for studying protein–protein interactions analogous to immunoprecipitation, using (instead of antibody) one of the interacting proteins (the “bait”) immobilised at a surface to capture the other protein (the “prey”).
Specifically-designed ssDNA (alternatively, RNA or a synthetic nucleic acid analogue, such as LNA or PNA) with a defined (known) nucleotide sequence used to detect complementary DNA or RNA sequence in a sample.
Reporter probe is usually labelled (radioactively, immunologically, or by fluorescent, electroactive, or other species to produce a specific signal upon hybridization).
Similar to capture probes, nucleic acid signalling probes (or nucleic acid aptamers) can be applied in studies of nucleic acid interactions with proteins and other ligands.
Binding of proteins to specific sites in DNA based on the precise recognition of nucleotide sequence and/or conformation of the DNA.
Sequence-specific DNA binding is typical for restriction enzymes, transcription factors and other proteins involved in cellular regulation, etc.
Attractive interaction between planar aromatic rings, in nucleic acids being one of the critical forces stabilizing double- and multistranded structures.
Stacking interactions are involved in binding of intercalators to DNA.
Method for the determination of strand breaks and DNA fragmentation in cells based on labelling and quantification of free 3′-OH ends of DNA.
The abbreviation is for terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL).
A molecular biology method for studying protein–protein or protein–DNA interactions in cellular (yeast or bacterial) milieu.
This method involves a transcription factor split into two separate domains (DNA binding and transcription activating), one of which is fused with one of the tested proteins (the “bait”) and the other with another tested protein (the “prey”), as well as with a reporter gene construct. Only upon physical interaction between bait and prey is the expression of the reporter gene observed.
activated nucleotide sugar 4.7.1
activator (in protein binding) 4.2.1
adiposomes. See lipid droplets 4.8.10
affinity (in immunology) 4.3.2
agglutination inhibition 4.3.4
alkaline degradation (in lipidomics) 4.8.1
alkaline hydrolysis. See alkaline degradation (in lipidomics) 4.8.1
allosteric regulation. See allostery 4.2.2
alternative splicing 4.5.1
amniotic fluid 3.1
amplification of DNA 4.4.1
anomeric hydroxy(l) group 4.7.4
antibody (Ab) 4.3.5
antigen (Ag) 4.3.6
antigenic determinant 4.3.7
assay kit 4.1.2
base pair (bp) 4.4.3
base sequence 4.4.4
base sequence analysis 4.4.5
basic local alignment search tool (BLAST) 4.4.6
binding affinity. See affinity (in immunology) 4.3.2
binding capacity 4.3.10
bioanalytical chemistry 2.1
biochemical receptor. See biological recognition element 4.1.5
biocomponent, at a biosensor. See biological recognition element 4.1.5
biological recognition element 4.1.5
blinding capacity 4.3.10
blood cell 3.3
blood cell count 3.4
body fluids 3.6
blood group 3.5
bottom-up proteomics 4.5.2
bound/free ration (in immunoassay) (B/F) 4.3.12
C-terminal analysis 4.5.3
capture probe 5.1
carbohydrate. See glycan 4.7.9
carbohydrate-binding protein 4.7.6
carbohydrate-binding protein. See glycan-binding protein 4.7.10
carrier protein 4.3.13
catalytic activity (in enzymology) 4.2.4
catalytic activity concentration 4.2.5
catalytic activity content 4.2.6
catalytic activity fraction 4.2.7
catalytic concentration. See catalytic activity concentration 4.2.5
cerebrospinal fluid (CSF) 3.7
chromatin immunoprecipitation 5.2
cloning vector 4.4.10
collision-induced dissociation (CID) (in proteomics) 4.5.5
comparative glycoproteomics 4.7.7
comparative proteoglycomics 4.7.8
complement (in immunology) 4.3.14
complementary DNA (cDNA) 4.4.11
complementary sequence 4.4.12
complete genome sequence 4.4.13
cord blood 3.8
core oligosaccharide 4.8.2
cross reactivity (in immunology) 4.3.16
cross-linking (in biomolecules) 5.3
cultivation (in metabolomics) 4.6.1
damage to DNA 4.4.14
damage. See damage to DNA 4.4.14
database searching (in proteomics) 4.5.6
denaturation of protein 4.2.9
deoxyribonucleic acid (DNA) 4.4.18
design of experiment (in metabolomics) 4.6.2
difference gel electrophoresis (DIGE) (in proteomics) 4.5.7
differential proteomics 4.5.8
disulfide bond cleavage 4.5.9
DNA fragmentation 4.4.19
DNA fragmentation index (DFI) 4.4.20
DNA integrity index 4.4.21
DNA mismatch 4.4.22
DNA profiling 4.4.23
DNA replication 4.4.24
DNA sequencing 4.4.25
double helix 4.4.26
Eadie-Hofstee plot 4.2.10
Edman degradation 4.5.10
electron-transfer dissociation (ETD) (in proteomics) 4.5.11
electron-transfer/high-energy collision dissociation (EthcD) (in proteomics) 4.5.12
electrospray ionisation (ESI) (in proteomics) 4.5.13
enzymatic decomposition 4.1.8
enzyme activity. See catalytic activity (in enzymology) 4.2.4
enzyme catalytic activity. See catalytic activity (in enzymology) 4.2.4
enzyme conjugate 4.3.17
epitope. See antigenic determinant 4.3.7
exogenous DNA 4.4.28
expression proteomics 4.5.14
fatty acids 4.8.4
fatty acyls (FA) 4.8.5
fermentation (in metabolomics) 4.6.6
fingerprinting (in metabolomics) 4.6.7
fluorescent in situ hybridization (FISH) 5.4
footprinting (in metabolomics) 4.6.9
functional proteomics 4.5.15
gel electrophoresis (1D PAGE) (in proteomics) 4.5.16
gene expression 4.4.31
glycan microarray 4.7.10
glycan profiling 4.7.11
glycan-binding protein 4.7.12
glycerolipids (GL) 4.8.6
glycerophospholipids (GP) 4.8.7
glycosaminoglycan (GAG) 4.7.22
glycosidic hydroxy group. See anomeric hydroxy(l) group 4.7.25
glycosidic linkage 4.7.26
groove binding (in DNA) 5.5
haematopoietic cell. See blood cell 3.3
Hanes-Woolf plot 4.2.13
Hansch analysis 4.1.9
hematocyte. See blood cell 3.3
hemocyte. See blood cell 3.3
higher-energy collision dissociation (HCD) (in proteomics) 4.5.17
hybridization (nucleic acids) 5.6
hybridization assay 5.7
immobilization (in bioassay and biosensors) 4.1.11
immune response 4.3.21
immunochemical specificity 4.3.24
immunoglobulin (Ig) 4.3.28
immunoglobulin class 4.3.29
indirect agglutination 4.3.33
intercalation (in biomolecules) 5.10
intermolecular interactions (in biomacromolecules) 5.11
intramolecular interaction (in biomacromolecules) 5.12
isoelectric focusing (IEF) (in proteomics) 4.5.18
lateral flow test 4.3.34
lectin microarray 4.7.34
ligand (in bioanalysis) 4.1.13
Lineweaver-Burk plot 4.2.17
lipid A 4.8.9
lipid bodies. See lipid droplets 4.8.10
lipid droplets 4.8.10
lipid extraction 4.8.11
lipid mediators. Signalling lipids See 4.8.31
lipid particles. See lipid droplets 4.8.10
lipid profiling 4.8.12
lipid remodelling 4.8.13
lipooligosaccharide (LOS) 4.8.17
lipopolysaccharide (LPS) 4.8.18
marker. See biomarker 4.1.6
mass fingerprinting (in proteomics) 4.5.19
mass mapping. See mass fingerprinting (in proteomics) 4.5.19
membrane bilayer 4.8.20
membrane rafts 4.8.21
metabolic pathway 4.6.11
metabolism quenching 4.6.13
metabolite fingerprinting and footprinting 4.6.15
metabolite profiling 4.6.16
Michaelis-Menten equation 4.2.18
molar catalytic activity 4.2.19
molecular shape of lipids 4.8.22
MS/MS data base identification (in proteomics) 4.5.20
multi-base mismatch 4.4.36
multi-dimensional protein identification technology (MudPIT) 4.5.21
N-terminal analysis 4.5.22
non-covalent interactions (in biomolecules) 5.13
non-specific binding (in DNA-proteins interactions) 5.14
Northern blot 4.4.39
nucleic acid 4.4.40
nucleic acid aptamers 4.4.41
nucleic acid-protein interaction 5.15
nucleobase lesion 4.4.43
nucleotide sequence 4.4.46
nucleotide sugar 4.7.36
occult blood 3.10
off peptide product ions 4.5.24
off-gel isoelectric focusing 4.5.25
oil bodies. See lipid droplets 4.8.10
oleosomes. See lipid droplets 4.8.10
open reading frame (ORF) 4.4.48
passive agglutination. See indirect agglutination 4.3.32
peptide de novo sequencing 4.5.27
peptide fragment ion 4.5.28
peptide fragmentation technique 4.5.29
peptide mass fingerprinting. See mass fingerprinting (in proteomics) 4.5.19
peptide nucleic acid (PNA) 4.4.49
peptide precursor ion 4.5.30
peripheral blood 3.11
phospholipids. See glycerophospholipids (GP) 4.8.6
plasma lipoproteins 4.8.24
point mutations. See single nucleotide polymorphisms (SNPs) 4.4.73
polyketides (PK) 4.8.25
polymerase chain reaction (PCR) 4.4.51
polymerase, DNA or RNA 4.4.52
polysaccharide. See glycan 4.7.9
polyunsaturated fatty acids (PUFA) 4.8.26
prenol lipids (PR) 4.8.27
primary metabolites 4.6.20
primary protein structure 4.5.34
probe, in genomics 4.4.54
protein complex 4.5.36
protein complex purification 4.5.37
protein database 4.5.38
protein-free filtrate 3.13
protein folding 4.5.39
protein fractionation 4.5.40
protein fragmentation 4.5.41
protein identification 4.5.42
protein machine 4.5.43
protein primary structure 4.5.44
protein purification 4.5.45
protein quantitation 4.5.46
protein separation. See protein fractionation 4.5.40
protein sequencer 4.5.47
protein sequencing 4.5.48
protein staining 4.5.49
protein-protein interaction (PPI) 5.16
proteolytic digestion 4.5.53
proteolytic enzyme 4.5.54
proteolytic peptide 4.5.55
pull-down assay 5.17
quantitative PCR (qPCR) 4.4.57
quaternary protein structure 4.5.58
real-time PCR 4.4.58
recombinant DNA 4.4.59
recombinant DNA technology 4.4.60
relative quantification (in proteomics) 4.5.59
reporter (signalling) probe 5.18
response time (of biosensor) 4.1.17
restriction endonuclease. See restriction enzyme 4.4.63
restriction enzyme 4.4.63
restriction fragment length polymorphism (RFLP) 4.4.64
reverse passive agglunation 4.3.38
reverse transcriptase 4.4.65
ribonucleic acid (RNA) 4.4.66
ribosomal RNA (rRNA) 4.4.68
saccharide. See glycan 4.7.9
saccharolipids (SL) 4.8.29
sample quality control 4.1.18
sandwich immunoassay 4.3.39
Sanger sequencing 4.4.70
secondary metabolites 4.6.21
secondary protein structure 4.5.60
shotgun lipidomics 4.8.30
shotgun method 4.4.71
signalling lipids 4.8.31
single mismatch 4.4.72
single nucleotide polymorphisms (SNPs) 4.4.73
Southern blot 4.4.74
specific binding (in DNA-protein interactions) 5.19
specific enzyme activity 4.2.20
specificity. See immunochemical specificity 4.3.24
sphingolipids (SP) 4.8.32
stable isotope labelling (in proteomics) 4.5.61
stacking interactions 5.20
steady-state response time (of biosensor) 4.1.21
sterols. See sterol lipids 4.8.33
sterol lipids 4.8.33
strand break 4.4.75
structural lipids 4.8.34
structural proteomics 4.5.62
tandem repeat sequences 4.4.76
targeted lipidomics 4.8.35
targeted proteomics 4.5.63
tertiary structure of a protein 4.5.64
top-down proteomics 4.5.65
tracer. See label 4.1.12
transducer (at biosensor) 4.1.22
transient response time (of biosensor) 4.1.23
trypsin (in proteomics) 4.5.66
TUNEL test 5.21
two hybrid system 5.22
two-dimensional gel electrophoresis (2D PAGE) (in proteomics) 4.5.67
two-site, non-competitive immunoassay. See sandwich immunoassay 4.3.38
unsaturated index (UI) 4.8.36
Western blot 4.5.68
yeast artificial chromosome (YAC) 4.4.79
1D PAGE. See gel electrophoresis (in proteomics) 4.5.16
2D PAGE. See two-dimensional gel electrophoresis (in proteomics) 4.5.16
Ab. See antibody 4.3.5
Ag. See antigen 4.3.6
B/F. See bound/free ratio (in immunoassay) 4.3.12
BLAST. See basic local alignment search tool 4.4.6
bp. See base pair 4.4.3
cDNA. See complementary DNA 4.4.11
CID. See collision-induced dissociation (in proteomics) 4.5.5
CSF. See cerebrospinal fluid 3.7
DFI. See DNA fragmentation index 4.4.20
DIGE. See difference gel electrophoresis (in proteomics) 4.5.7
DNA. See deoxyribonucleic acid 4.4.18
ESI. See electrospray ionisation (in proteomics) 4.5.13
ETD. See electron-transfer dissociation (in proteomics) 4.5.11
EthcD. See electron-transfer/higher-energy collision dissociation (in proteomics) 4.5.12
FA. See fatty acyls 4.8.5
FISH. See fluorescent in situ hybridization 5.4
GAG. See glucosaminoglycan 4.7.22
GL. See glycerolipids 4.8.6
GP. See glycerophospholipids 4.8.7
HCD. See higher-energy collision dissociation (in proteomics) 4.5.17
IEF. See isoelectric focusing (in proteomics) 4.5.18
Ig. See immunoglobulin 4.3.28
LNA. See double helix 4.4.26
LOS. See lipooligosaccharide 4.8.17
LPS. See lipopolysaccharide 4.8.18
MudPIT. See multidimensional protein identification technology 4.5.21
OFFGELTM. See off-gel isoelectric focusing 4.5.24
ORF. See open reading frame 4.4.48
PCR. See polymerase chain reaction 4.4.51
PK. See polyketides 4.8.25
PNA. See peptide nucleic acid 4.4.49
PPI. See protein-protein interaction 5.16
PR. See prenol lipids 4.8.25
PUFA. See polyunsaturated fatty acids 4.8.26
qPCR. See quantitative PCR 4.4.58
RFLP. See restriction fragment length polymorphism 4.4.64
RNA. See ribonucleic acid 4.4.66
rRNA. See ribosomal RNA 4.4.68
SL. See saccharolipids 4.8.29
SNPs. See single nucleotide polymorphisms 4.4.73
SP. See sphingolipids 4.8.32
ST. See sterol lipids 4.8.33
UI. See unsaturation index 4.8.36
YAC. See yeast artificial chromosome 4.4.79
Membership of the IUPAC Analytical Chemistry Division for the period 2014–2015 was as follows:
President: D. Brynn Hibbert (Australia); Secretary: Z. Mester (Canada); Vice President: J. Labuda (Slovakia); Past President: M. Filomena Camões (Portugal); Titular Members: C. Balarew (Bulgaria); Y. Chen (China); A. Felinger (Hungary); H. Kim (South Korea); C. Magalhães (Portugal); H. M. M. Sirén (Finland); Associate Members: R. Apak (Turkey); P. Bode (The Netherlands); D. Craston (UK); Y. Heng Lee (Malaysia); T. Maryutina (Russia); N. Torto (South Africa); National Representatives: P. DeBièvre (Belgium); M. N. Eberlin (Brazil); P. Novak (Croatia); L. Charles (France); D. Mandler (Israel); J. Hanif (Pakistan); A. Fajgelj (Slovenia); O. Chande Othman (Tanzania); K. Grudpan (Thailand); D. G. Shaw (USA).
Funding: International Union of Pure and Applied Chemistry, Funder Id: 10.13039/100006987, Grant Number: 2011-047-1-500: Recent advances in bioanalytical chemistry: characterization and classification.
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