english Icono del idioma   español Icono del idioma  

Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12008/30819 How to cite
Title: Reduction of sulfenic acids by ascorbate in proteins, connecting thiol-dependent to alternative redox pathways
Authors: Anschau, V.
Ferrer-Sueta, Gerardo
Aleixo-Silva, R. L.
Fernandes, R. B.
Tairum, C. A.
Tonoli, C. C. C.
Murakami, M. T.
Oliveira, M. A. de
Netto, Luis E. S.
Type: Artículo
Keywords: Ascorbate, Peroxiredoxin, Sulfenic acid, Peroxides
Issue Date: 2020
Abstract: Sulfenic acids are the primary product of thiol oxidation by hydrogen peroxide and other oxidants. Several aspects of sulfenic acid formation through thiol oxidation were established recently. In contrast, the reduction of sulfenic acids is still scarcely investigated. Here, we characterized the kinetics of the reduction of sulfenic acids by ascorbate in several proteins. Initially, we described the crystal structure of our model protein (Tsa2-C170S). There are other Tsa2 structures in distinct redox states in public databases and all of them are decamers, with the peroxidatic cysteine very accessible to reductants, convenient features to investigate kinetics. We determined that the reaction between Tsa2-C170S-Cys-SOH and ascorbate proceeded with a rate constant of 1.40 ± 0.08 × 103 M−1 s−1 through a competition assay developed here, employing 2,6–dichlorophenol-indophenol (DCPIP). A series of peroxiredoxin enzymes (Prx6 sub family) were also analyzed by this competition assay and we observed that the reduction of sulfenic acids by ascorbate was in the 0.4–2.2 × 103 M−1 s−1 range. We also evaluated the same reaction on glyceraldehyde 3-phosphate dehydrogenase and papain, as the reduction of their sulfenic acids by ascorbate were reported previously. Once again, the rate constants are in the 0.4–2.2 × 103 M−1 s−1 range. We also analyzed the reduction of Tsa2-C170S-SOH by ascorbate by a second, independent method, following hydrogen peroxide reduction through a specific electrode (ISO-HPO-2, World Precision Instruments) and employing a bi-substrate, steady state approach. The was 7.4 ± 0.07 × 103 M−1 s−1, which was in the same order of magnitude as the value obtained by the DCPIP competition assay. In conclusion, our data indicates that reduction of sulfenic acid in various proteins proceed at moderate rate and probably this reaction is more relevant in biological systems where ascorbate concentrations are high.
Publisher: Elsevier
IN: Free Radical Biology and Medicine, 2020, 156: 207-216
DOI: 10.1016/j.freeradbiomed.2020.06.015
ISSN: 0891-5849
Citation: Anschau, V, Ferrer-Sueta, G, Aleixo-Silva, R, [y otros] "Reduction of sulfenic acids by ascorbate in proteins, connecting thiol-dependent to alternative redox pathways". Free Radical Biology and Medicine. [en línea] 2020, 156: 207-216. 10 h. DOI: 10.1016/j.freeradbiomed.2020.06.015
License: Licencia Creative Commons Atribución (CC - By 4.0)
Appears in Collections:Publicaciones académicas y científicas - Facultad de Ciencias

Files in This Item:
File Description SizeFormat  
10.1016j.freeradbiomed.2020.06.015.pdf3,6 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons