Analysis of Cysteine Post Translational Modifications Using Organic Mercury Resin

Curr Protoc Protein Sci. 2018 Nov;94(1):e69. doi: 10.1002/cpps.69. Epub 2018 Oct 3.

Abstract

The wide reactivity of the thiol group enables the formation of a variety of reversible, covalent modifications on cysteine residues. S-nitrosylation, like many other post-translational modifications, is site selective, reversible, and necessary for a wide variety of fundamental cellular processes. The overall abundance of S-nitrosylated proteins and reactivity of the nitrosyl group necessitates an enrichment strategy for accurate detection with adequate depth. Herein, a method is presented for the enrichment and detection of endogenous protein S-nitrosylation from complex mixtures of cell or tissue lysate utilizing organomercury resin. Minimal adaptations to the method also support the detection of either S-glutathionylation or S-acylation using the same enrichment platform. When coupled with high accuracy mass spectrometry, these methods enable a site-specific level of analysis, facilitating the curation comparable datasets of three separate cysteine post-translational modifications. © 2018 by John Wiley & Sons, Inc.

Keywords: S-acylation; cysteine; glutathionylation; nitrosylation; proteomics; signaling.

Publication types

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

MeSH terms

  • Animals
  • Cysteine / analysis*
  • Cysteine / chemistry
  • Humans
  • Organomercury Compounds / chemistry*
  • Protein Processing, Post-Translational*
  • Resins, Synthetic / chemistry*

Substances

  • Organomercury Compounds
  • Resins, Synthetic
  • Cysteine