Activity-based probes as a tool for functional proteomic analysis of proteases

Expert Rev Proteomics. 2008 Oct;5(5):721-30. doi: 10.1586/14789450.5.5.721.

Abstract

Traditional proteomics methodology allows global analysis of protein abundance but does not provide information on the regulation of protein activity. Proteases, in particular, are known for their multilayered post-translational activity regulation that can lead to a significant difference between protease abundance levels and their enzyme activity. To address these issues, the field of activity-based proteomics has been established in order to characterize protein activity and monitor the functional regulation of enzymes in complex proteomes. In this review, we present structural features of activity-based probes for proteases and discuss their applications in proteomic profiling of various catalytic classes of proteases.

Publication types

  • Review

MeSH terms

  • Cysteine Endopeptidases / chemistry
  • Cysteine Endopeptidases / metabolism
  • Metalloproteases / chemistry
  • Metalloproteases / metabolism
  • Molecular Probes / chemistry*
  • Molecular Structure
  • Peptide Hydrolases / chemistry
  • Peptide Hydrolases / metabolism*
  • Proteomics / methods*
  • Serine Endopeptidases / chemistry
  • Serine Endopeptidases / metabolism

Substances

  • Molecular Probes
  • Metalloproteases
  • Peptide Hydrolases
  • Serine Endopeptidases
  • Cysteine Endopeptidases