N-Terminomics Strategies for Protease Substrates Profiling

Molecules. 2021 Aug 3;26(15):4699. doi: 10.3390/molecules26154699.

Abstract

Proteases play a central role in various biochemical pathways catalyzing and regulating key biological events. Proteases catalyze an irreversible post-translational modification called proteolysis by hydrolyzing peptide bonds in proteins. Given the destructive potential of proteolysis, protease activity is tightly regulated. Dysregulation of protease activity has been reported in numerous disease conditions, including cancers, neurodegenerative diseases, inflammatory conditions, cardiovascular diseases, and viral infections. The proteolytic profile of a cell, tissue, or organ is governed by protease activation, activity, and substrate specificity. Thus, identifying protease substrates and proteolytic events under physiological conditions can provide crucial information about how the change in protease regulation can alter the cellular proteolytic landscape. In recent years, mass spectrometry-based techniques called N-terminomics have become instrumental in identifying protease substrates from complex biological mixtures. N-terminomics employs the labeling and enrichment of native and neo-N-termini peptides, generated upon proteolysis followed by mass spectrometry analysis allowing protease substrate profiling directly from biological samples. In this review, we provide a brief overview of N-terminomics techniques, focusing on their strengths, weaknesses, limitations, and providing specific examples where they were successfully employed to identify protease substrates in vivo and under physiological conditions. In addition, we explore the current trends in the protease field and the potential for future developments.

Keywords: CHOPS; COFRADIC; N-terminomics; TAILS; protease substrates; subtiligase.

Publication types

  • Review

MeSH terms

  • Humans
  • Mass Spectrometry
  • Peptide Hydrolases / chemistry*
  • Peptides / chemistry*
  • Proteolysis*
  • Proteomics*
  • Substrate Specificity

Substances

  • Peptides
  • Peptide Hydrolases