Elucidating Citrullination by Mass Spectrometry and Its Role in Disease Pathogenesis

J Proteome Res. 2021 Jan 1;20(1):38-48. doi: 10.1021/acs.jproteome.0c00474. Epub 2020 Oct 5.

Abstract

This review focuses on discussing key mechanisms in disease pathogenesis mediated by the protein post-translational modification citrullination. These processes are discussed in depth in the context of complex diseases such as rheumatoid arthritis, cancer, central nervous system disorders, and cardiovascular disease. Additionally, a critical evaluation of challenges in laboratory detection of citrullination sites is also outlined. In this context, the role of mass spectrometry is discussed with a focus on contemporary techniques that offer promising options to detect the exact site of protein citrullination. Novel methods described in the paper have the potential to detect and quantify the occurrence of post-translational modification sites for diagnosis and therapeutic purposes with a high degree of specificity and sensitivity. Furthermore, they offer a much faster performance than traditional techniques making them ideal for large-scale experimentation.

Keywords: CNS; atherosclerosis; cancer; cardiac disease; citrullination; mass spectrometry; rheumatoid arthritis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Arthritis, Rheumatoid*
  • Citrullination*
  • Citrulline / metabolism
  • Humans
  • Mass Spectrometry
  • Protein Processing, Post-Translational
  • Protein-Arginine Deiminases

Substances

  • Citrulline
  • Protein-Arginine Deiminases