Redox albuminomics: oxidized albumin in human diseases

Antioxid Redox Signal. 2012 Dec 1;17(11):1515-27. doi: 10.1089/ars.2012.4702. Epub 2012 Jun 25.


Significance: Albumin is the major contributor to colloid oncotic pressure and also serves as an important carrier protein of many endogenous and exogenous molecules throughout the body. In blood and extravascular fluids, albumin is susceptible to different oxidative modifications, especially thiol oxidation and carbonylation. Because of its metal-binding properties and the redox properties of its Cys34 thiol, albumin displays an important antioxidant activity. As albumin is the predominant protein in most body fluids, its Cys34 represents the largest fraction of free thiols within body fluids.

Recent advances: Evidence that albumin oxidation takes place in vivo has been reported only recently. Different redox proteomic, mass spectrometric, and chromatographic techniques have shown albumin redox modifications in various human pathophysiological conditions. As a whole, most data here presented demonstrate that massive albumin oxidation occurs in vivo in different biological fluids and, to some extent, that this process is correlated to organ dysfunction.

Critical issues: Recent reports suggest that the albumin redox state may serve as a global biomarker for the redox state in the body in various human diseases. However, further study is required to elucidate the exact relationship between albumin oxidation and pathology. In addition, it is unknown if some albumin oxidized forms may also have diagnostic uses.

Future directions: Application of specific redox proteomics techniques for the characterization of oxidized albumin forms in screening studies is required. A further challenge will be to analyze how these oxidative albumin modifications are related to real impact to the body.

Publication types

  • Review

MeSH terms

  • Albumins* / chemistry
  • Albumins* / metabolism
  • Antioxidants / metabolism
  • Body Fluids / chemistry
  • Body Fluids / metabolism
  • Humans
  • Inflammation* / metabolism
  • Inflammation* / physiopathology
  • Oxidation-Reduction
  • Oxidative Stress*
  • Protein Carbonylation*
  • Proteins / metabolism
  • Sulfhydryl Compounds / chemistry


  • Albumins
  • Antioxidants
  • Proteins
  • Sulfhydryl Compounds