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Improved integrative analysis of the thiol redox proteome using filter-aided sample preparation.

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Date

2019-12-20

Authors

Bonzon-Kulichenko, Elena
Camafeita, Emilio
Lopez, Juan Antonio
Gomez-Serrano, Maria
Jorge, Inmaculada
Calvo, Enrique
Nuñez, Estefania
Trevisan-Herraz, Marco
Bagwan, Navratan
Barcena, Jose Antonio

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Elsevier
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Abstract

Changes in the oxidation state of protein Cys residues are involved in cell signalling and play a key role in a variety of pathophysiological states. We had previously developed GELSILOX, an in-gel method that enables the large-scale, parallel analysis of dynamic alterations to the redox state of Cys sites and protein abundance changes. Here we present FASILOX, a further development of the GELSILOX approach featuring: i) significantly increased peptide recovery, ii) enhanced sensitivity for the detection of Cys oxidative alterations, and iii) streamlined workflow that results in shortened assay duration. In mitochondria isolated from the adipose tissue of obese, diabetic patients, FASILOX revealed a sexually dimorphic trait of Cys oxidation involving mainly mitochondrial oxidative phosphorylation complexes. These results provide the first evidence for a decreased efficiency in the antioxidant response of men as compared to women.

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Female
Humans
Male
Oxidation-reduction
Peptides
Protein processing, post-translational
Proteome
Sulfhydryl compounds

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Compuestos de sulfhidrilo
Oxidación-reducción
Procesamiento proteico-postraduccional
Proteoma
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Keywords

Adipose tissue, Cys oxidation, FASILOX, Filter-aided sample preparation, Sexual dimorphism, Thiol redox proteome

Citation

Bonzon-Kulichenko E, Camafeita E, López JA, Gómez-Serrano M, Jorge I, Calvo E, et al. Improved integrative analysis of the thiol redox proteome using filter-aided sample preparation. J Proteomics. 2020 Mar 1;214:103624