Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Apr;54(4):559-573.
doi: 10.1007/s00726-021-03085-6. Epub 2021 Oct 20.

Protein carbonylation in food and nutrition: a concise update

Affiliations

Protein carbonylation in food and nutrition: a concise update

Mario Estévez et al. Amino Acids. 2022 Apr.

Abstract

Protein oxidation is a topic of indisputable scientific interest given the impact of oxidized proteins on food quality and safety. Carbonylation is regarded as one of the most notable post-translational modifications in proteins and yet, this reaction and its consequences are poorly understood. From a mechanistic perspective, primary protein carbonyls (i.e. α-aminoadipic and γ-glutamic semialdehydes) have been linked to radical-mediated oxidative stress, but recent studies emphasize the role alternative carbonylation pathways linked to the Maillard reaction. Secondary protein carbonyls are introduced in proteins via covalent linkage of lipid carbonyls (i.e. protein-bound malondialdehyde). The high reactivity of protein carbonyls in foods and other biological systems indicates the intricate chemistry of these species and urges further research to provide insight into these molecular mechanisms and pathways. In particular, protein carbonyls are involved in the formation of aberrant and dysfunctional protein aggregates, undergo further oxidation to yield carboxylic acids of biological relevance and establish interactions with other biomolecules such as oxidizing lipids and phytochemicals. From a methodological perspective, the routine dinitrophenylhydrazine (DNPH) method is criticized not only for the lack of accuracy and consistency but also authors typically perform a poor interpretation of DNPH results, which leads to misleading conclusions. From a practical perspective, the biological relevance of protein carbonyls in the field of food science and nutrition is still a topic of debate. Though the implication of carbonylation on impaired protein functionality and poor protein digestibility is generally recognized, the underlying mechanism of such connections requires further clarification. From a medical perspective, protein carbonyls are highlighted as markers of protein oxidation, oxidative stress and disease. Yet, the specific role of specific protein carbonyls in the onset of particular biological impairments needs further investigations. Recent studies indicates that regardless of the origin (in vivo or dietary) protein carbonyls may act as signalling molecules which activate not only the endogenous antioxidant defences but also implicate the immune system. The present paper concisely reviews the most recent advances in this topic to identify, when applicable, potential fields of interest for future studies.

Keywords: Disease; Maillard reaction; Nutrition; Oxidative stress; Protein carbonylation; Protein oxidation; Safety; α-Aminoadipic acid; α-Aminoadipic semialdehyde.

PubMed Disclaimer

Conflict of interest statement

The authors have no conflicts of interest to declare that are relevant to the content of this article.

Figures

Fig. 1
Fig. 1
Mechanisms of primary carbonylation: formation of α-aminoadipic acid (α-AS). A Radical-mediated oxidative deamination of protein-bound lysine; B Maillard-mediated oxidative deamination of protein-bound lysine
Fig. 2
Fig. 2
Mechanisms of secondary carbonylation. A Michael addition of 4-hydroxynonenal to protein-bound lysine; B Michael addition of malondialdehyde to protein-bound lysine
Fig. 3
Fig. 3
Illustration of the overestimation of primary carbonylation in malondialdehyde-exposed proteins by the dinitrophenylhydrazine method as reported by Estévez et al. (2019). A-quadrant occurrence of protein-bound lysine and α-AS residues, B-quadrant addition of malondialdehyde to protein-bound lysine residues, C-quandrant derivatization of protein-bound α-AS residues by the dinitrophenylhydrazine, D-quadrant derivatization of protein-bound α-AS and malondialdehyde residues by the dinitrophenylhydrazine
Fig. 4
Fig. 4
Mechanisms of the cytotoxic effects of α-AA on CACO-2 cells as reported by Díaz-Velasco et al. (2020)

Similar articles

Cited by

References

    1. Akagawa M. Protein carbonylation: molecular mechanisms, biological implications, and analytical approaches. Free Radic Res. 2020 doi: 10.1080/10715762.2020.1851027. - DOI - PubMed
    1. Akagawa M, Sasaki D, Kurota Y, Suyama K. Formation of α-aminoadipic and γ-glutamic semialdehydes in proteins by the Maillard reaction. Ann NY Acad Sci. 2005;1043:129–134. doi: 10.1196/annals.1333.016. - DOI - PubMed
    1. Akagawa M, Sasaki D, Ishii Y, et al. New method for the quantitative determination of major protein carbonyls, α-aminoadipic and γ-glutamic semialdehydes: Investigation of the formation mechanism and chemical nature in vitro and in vivo. Chem Res Toxicol. 2006;19:1059–1065. doi: 10.1021/tx060026p. - DOI - PubMed
    1. Akagawa M, Suyama K, Uchida K. Fluorescent detection of α-aminoadipic and γ-glutamic semialdehydes in oxidized proteins. Free Radic Biol Med. 2009;46:701–706. doi: 10.1016/j.freeradbiomed.2008.12.014. - DOI - PubMed
    1. Alomari E, Bruno S, Ronda L, et al. Protein carbonylation detection methods: a comparison. Data Brief. 2018;19:2215–2220. doi: 10.1016/j.dib.2018.06.088. - DOI - PMC - PubMed

LinkOut - more resources

-