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Publication Date:
December 2008
ISSN:
1437-4315
DOI:
10.1515/BC.2009.026

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A completed KLK activome profile: investigation of activation profiles of KLK9, 10, and 15

Hyesook Yoon1 / Sachiko I. Blaber2 / Mekdes Debela3 / Peter Goettig4 / Isobel A. Scarisbrick5 / Michael Blaber6

1Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306-4300, USA

2Department of Biomedical Sciences, Florida State University, Tallahassee, FL 32306-4300, USA

3Max Planck Institute for Biochemistry, Proteinase Research Group, Am Klopferspitz 18, D-82152 Martinsried, Germany

4Max Planck Institute for Biochemistry, Proteinase Research Group, Am Klopferspitz 18, D-82152 Martinsried, Germany and Structural Biology Group, Department of Molecular Biology, University of Salzburg, A-5020 Salzburg, Austria

5Program for Molecular Neuroscience and Departments of Neurology, and Physical Medicine and Rehabilitation, Mayo Medical and Graduate Schools, Rochester, MN 55905, USA

6Department of Biomedical Sciences, Florida State University, Tallahassee, FL 32306-4300, USA

Corresponding author

Citation Information: Biological Chemistry. Volume 390, Issue 4, Pages 373–377, ISSN (Online) 1437-4315, ISSN (Print) 1431-6730, DOI: 10.1515/BC.2009.026, December 2008

Publication History:
Received:
2008-10-28
Accepted:
2008-11-29
Published Online:
2008-12-17

Abstract

We previously reported the activation profiles of the human kallikrein-related peptidases (KLKs) as determined from a KLK pro-peptide fusion-protein system. That report described the activity profiles of 12 of the 15 mature KLKs versus the 15 different pro-KLK sequences. The missing profiles in the prior report, involving KLK9, 10, and 15, are now described. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis, mass spectrometry, and N-terminal sequence analyses show that KLK9 and 10 exhibit low hydrolytic activities towards all of the 15 pro-KLK sequences, while KLK15 exhibits significant activity towards both Arg- and Lys-containing KLK pro-sequences. The ability of KLK15 to activate pro-KLK8, 12, and 14 is confirmed using recombinant pro-KLK proteins, and shown to be significant for activation of pro-KLK8 and 14, but not 12. These additional data for KLK9, 10, and 15 now permit a completed KLK activome profile, using a KLK pro-peptide fusion-protein system, to be described. The results suggest that KLK15, once activated, can potentially feed back into additional pro-KLK activation pathways. Conversely, KLK9 and 10, once activated, are unlikely to participate in further pro-KLK activation pathways, although similar to KLK1 they may activate other bioactive peptides.

Keywords: activation cascade; activome; kallikrein; kallikrein-related peptidases (KLKs); protease

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