Chemical biology of protein citrullination by the protein A arginine deiminases

Curr Opin Chem Biol. 2021 Aug:63:19-27. doi: 10.1016/j.cbpa.2021.01.010. Epub 2021 Mar 4.

Abstract

Citrullination is a post-translational modification (PTM) that converts peptidyl-arginine into peptidyl-citrulline; citrullination is catalyzed by the protein arginine deiminases (PADs). This PTM is associated with several physiological processes, including the epigenetic regulation of gene expression, neutrophil extracellular trap formation, and DNA-damage induced apoptosis. Notably, aberrant protein citrullination is relevant to several autoimmune and neurodegenerative diseases and certain forms of cancer. As such, the PADs are promising therapeutic targets. In this review, we discuss recent advances in the development of PAD inhibitors and activity-based probes, the development and use of citrulline-specific probes in chemoproteomic applications, and methods to site-specifically incorporate citrulline into proteins.

Keywords: Activity-based protein profiling; Autocitrullination; Citrulline incorporation; Inhibitor; Post-translational modifications; Protein arginine deiminase (PAD).

Publication types

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

MeSH terms

  • Animals
  • Arginine / chemistry*
  • Autoimmune Diseases / metabolism
  • Catalysis
  • Citrullination
  • Citrulline / chemistry*
  • Epigenesis, Genetic
  • Humans
  • Neoplasms / metabolism
  • Neurodegenerative Diseases / metabolism
  • Protein Binding
  • Protein Conformation
  • Protein Processing, Post-Translational
  • Protein-Arginine Deiminases / metabolism*
  • Proteins / chemistry*

Substances

  • Proteins
  • Citrulline
  • Arginine
  • Protein-Arginine Deiminases