Protein carbonylation as a major hallmark of oxidative damage: update of analytical strategies

Mass Spectrom Rev. 2014 Mar-Apr;33(2):79-97. doi: 10.1002/mas.21381. Epub 2013 Jul 7.

Abstract

Protein carbonylation, one of the most harmful irreversible oxidative protein modifications, is considered as a major hallmark of oxidative stress-related disorders. Protein carbonyl measurements are often performed to assess the extent of oxidative stress in the context of cellular damage, aging and several age-related disorders. A wide variety of analytical techniques are available to detect and quantify protein-bound carbonyls generated by metal-catalyzed oxidation, lipid peroxidation or glycation/glycoxidation. Here we review current analytical approaches for protein carbonyl detection with a special focus on mass spectrometry-based techniques. The utility of several carbonyl-derivatization reagents, enrichment protocols and especially advanced mass spectrometry techniques are compared and discussed in detail. Furthermore, the mechanisms and biology of protein carbonylation are summarized based on recent high-throughput proteomics data.

Keywords: hydrazine; hydroxyl amine; mass spectrometry; protein carbonylation.

Publication types

  • Review

MeSH terms

  • Animals
  • Humans
  • Mass Spectrometry / methods*
  • Oxidation-Reduction
  • Oxidative Stress
  • Protein Carbonylation*
  • Proteins / chemistry*
  • Proteins / metabolism
  • Proteomics / methods

Substances

  • Proteins