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Publicly Available Published by De Gruyter January 1, 2009

Dynamic barriers and tunneling. New views of hydrogen transfer in enzyme reactions

  • J. P. Klinman

Abstract

Hydrogen-transfer processes are expected to show appreciable quantum mechanical behavior. Intensive investigations of enzymes under their physiological conditions show this to be true in practically every example investigated. Initially, tunneling was treated either as a tunneling correction [cf. Bell, The Tunnel Effect in Chemistry, Chapman & Hall, New York, (l980)], or as corner-cutting [Truhlar et al., J. Chem. Phys. 100, 12771 (l996)]. This worked well as long as the observed properties could be explained by “corrections” to transition-state theory. However, over the past several years, enzymatic behaviors have been observed that are so deviant as to lie outside of transition-state theory. This phenomenon is discussed in the context of the enzyme, soybean lipoxygenase. An environmentally coupled hydrogen-tunneling model is presented that derives from the treatments of Kuznetsov and Ullstrup [Can. J. Chem. 77, 689 (l999)], and includes heavy-atom reorganization (temperature-dependent and largely isotope-independent), together with heavy-atom gating (temperature- and isotope-dependent). This treatment can explain a wide range of behaviors and leads to a new view of the origin of kinetic isotope effects in hydrogen-transfer reactions. These properties link enzyme fluctuations to the hydrogen-transfer reaction coordinate, making a quantum view of H-transfer necessarily a dynamic view of catalysis.


Conference

International Conference on Physical Organic Chemistry (ICPOC-16): Structure and Mechanism in Organic Chemistry, International Conference on Physical Organic Chemistry, ICPOC, Physical Organic Chemistry, 16th, San Diego, California, USA, 2002-08-04–2002-08-09


Published Online: 2009-01-01
Published in Print: 2003-01-01

© 2013 Walter de Gruyter GmbH, Berlin/Boston

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