Multiplex substrate profiling by mass spectrometry for proteases

Methods Enzymol. 2023:682:375-411. doi: 10.1016/bs.mie.2022.09.009. Epub 2022 Dec 21.

Abstract

Proteolysis is a central regulator of many biological pathways and the study of proteases has had a significant impact on our understanding of both native biology and disease. Proteases are key regulators of infectious disease and misregulated proteolysis in humans contributes to a variety of maladies, including cardiovascular disease, neurodegeneration, inflammatory diseases, and cancer. Central to understanding a protease's biological role, is characterizing its substrate specificity. This chapter will facilitate the characterization of individual proteases and complex, heterogeneous proteolytic mixtures and provide examples of the breadth of applications that leverage the characterization of misregulated proteolysis. Here we present the protocol of Multiplex Substrate Profiling by Mass Spectrometry (MSP-MS), a functional assay that quantitatively characterizes proteolysis using a synthetic library of physiochemically diverse, model peptide substrates, and mass spectrometry. We present a detailed protocol as well as examples of the use of MSP-MS for the study of disease states, for the development of diagnostic and prognostic tests, for the generation of tool compounds, and for the development of protease-targeted drugs.

Keywords: Cancer; Diagnostics; Enzymology; Infectious disease; Mass spectrometry; Post-translational modifying enzymes; Prognostics; Proteases; Substrate profiling.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Endopeptidases / metabolism
  • Humans
  • Mass Spectrometry / methods
  • Peptide Hydrolases* / metabolism
  • Proteolysis
  • Proteomics* / methods
  • Substrate Specificity

Substances

  • Peptide Hydrolases
  • Endopeptidases