Rapid Assessment of Pepsin Column Activity for Reliable HDX-MS Studies

J Am Soc Mass Spectrom. 2021 Sep 1;32(9):2386-2390. doi: 10.1021/jasms.1c00080. Epub 2021 May 13.

Abstract

Hydrogen/deuterium exchange with mass spectrometry (HDX-MS) is a widely used technique to probe protein structural dynamics, track conformational changes, and map protein-protein interactions. Most HDX-MS studies employ a bottom-up approach utilizing the acid active protease pepsin to digest the protein of interest, often utilizing immobilized protease in a column format. The extent of proteolytic cleavage will greatly influence data quality and presents a major source of variation in HDX-MS studies. Here, we present a simple cocktail of commonly available peptides that are substrates of pepsin and can serve as a rapid check of pepsin column activity. The peptide-based assay requires no system modifications and provides an immediate readout to check and benchmark pepsin activity across different HDX-MS platforms.

Keywords: HDX-MS; digestion; hydrogen/deuterium exchange; mass spectrometry; pepsin; protease.

MeSH terms

  • Animals
  • Chromatography, Liquid / methods*
  • Enzymes, Immobilized* / chemistry
  • Enzymes, Immobilized* / metabolism
  • Hydrogen Deuterium Exchange-Mass Spectrometry / methods*
  • Pepsin A* / chemistry
  • Pepsin A* / metabolism
  • Peptide Fragments / analysis
  • Peptide Fragments / chemistry
  • Peptide Fragments / metabolism
  • Protein Conformation
  • Proteins / analysis
  • Proteins / chemistry
  • Proteins / metabolism
  • Reproducibility of Results
  • Swine

Substances

  • Enzymes, Immobilized
  • Peptide Fragments
  • Proteins
  • Pepsin A