Proteome-Scale Analysis of Protein S-Acylation Comes of Age

J Proteome Res. 2021 Jan 1;20(1):14-26. doi: 10.1021/acs.jproteome.0c00409. Epub 2020 Nov 30.

Abstract

Protein S-acylation (commonly known as palmitoylation) is a widespread reversible lipid modification, which plays critical roles in regulating protein localization, activity, stability, and complex formation. The deregulation of protein S-acylation contributes to many diseases such as cancer and neurodegenerative disorders. The past decade has witnessed substantial progress in proteomic analysis of protein S-acylation, which significantly advanced our understanding of S-acylation biology. In this review, we summarized the techniques for the enrichment of S-acylated proteins or peptides, critically reviewed proteomic studies of protein S-acylation at eight different levels, and proposed major challenges for the S-acylproteomics field. In summary, proteome-scale analysis of protein S-acylation comes of age and will play increasingly important roles in discovering new disease mechanisms, biomarkers, and therapeutic targets.

Keywords: ABE; APT; MLCC; PAT; S-acylation; S-palmitoylation; click chemistry; palmitoylation; proteomics.

Publication types

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

MeSH terms

  • Acylation
  • Lipoylation
  • Protein S
  • Proteome* / genetics
  • Proteome* / metabolism
  • Proteomics*

Substances

  • Protein S
  • Proteome