4.3 Article

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

Journal

BIOLOGICAL CHEMISTRY
Volume 390, Issue 4, Pages 373-377

Publisher

WALTER DE GRUYTER GMBH
DOI: 10.1515/BC.2009.026

Keywords

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

Funding

  1. NIH [1R15NS057771-01]
  2. National Multiple Sclerosis Society [PP1113, RG3367]
  3. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS052741, R15NS057771] Funding Source: NIH RePORTER

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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 prosequences. 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.

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