Characterization of In Vivo Protein Complexes via Chemical Cross-Linking and Mass Spectrometry

Anal Chem. 2022 Jan 25;94(3):1537-1542. doi: 10.1021/acs.analchem.1c02410. Epub 2021 Dec 28.

Abstract

Cells perform various functions by proteins via protein complexes. Characterization of protein complexes is critical to understanding their biological and clinical significance and has been one of the major efforts of functional proteomics. To date, most protein complexes are characterized by the in vitro system from protein extracts after the cells or tissues are lysed, and it has been challenging to determine which of these protein complexes are formed in intact cells. Herein, we report an approach to preserve protein complexes using in vivo cross-linking, followed by size exclusion chromatography and data-independent acquisition mass spectrometry. This approach enables the characterization of in vivo protein complexes from cells or tissues, which allows the determination of protein complexes in clinical research. More importantly, the described approach can identify protein complexes that are not detected by the in vitro system, which provide unique protein function information.

Publication types

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

MeSH terms

  • Chromatography, Gel
  • Cross-Linking Reagents / chemistry
  • Mass Spectrometry / methods
  • Proteins* / analysis
  • Proteomics* / methods

Substances

  • Cross-Linking Reagents
  • Proteins