english Icono del idioma   español Icono del idioma  

Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/20.500.12008/30819 Cómo citar
Registro completo de metadatos
Campo DC Valor Lengua/Idioma
dc.contributor.authorAnschau, V.-
dc.contributor.authorFerrer-Sueta, Gerardo-
dc.contributor.authorAleixo-Silva, R. L.-
dc.contributor.authorFernandes, R. B.-
dc.contributor.authorTairum, C. A.-
dc.contributor.authorTonoli, C. C. C.-
dc.contributor.authorMurakami, M. T.-
dc.contributor.authorOliveira, M. A. de-
dc.contributor.authorNetto, Luis E. S.-
dc.date.accessioned2022-02-10T14:26:22Z-
dc.date.available2022-02-10T14:26:22Z-
dc.date.issued2020-
dc.identifier.citationAnschau, 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.2020.06.015es
dc.identifier.issn0891-5849-
dc.identifier.urihttps://hdl.handle.net/20.500.12008/30819-
dc.description.abstractSulfenic 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.es
dc.format.extent10 h.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenes
dc.publisherElsevieres
dc.relation.ispartofFree Radical Biology and Medicine, 2020, 156: 207-216es
dc.rightsLas obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)es
dc.subjectAscorbatees
dc.subjectPeroxiredoxines
dc.subjectSulfenic acides
dc.subjectPeroxideses
dc.titleReduction of sulfenic acids by ascorbate in proteins, connecting thiol-dependent to alternative redox pathwayses
dc.typeArtículoes
dc.contributor.filiacionAnschau V.-
dc.contributor.filiacionFerrer-Sueta Gerardo, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Química Biológica.-
dc.contributor.filiacionAleixo-Silva R. L.-
dc.contributor.filiacionFernandes R. B.-
dc.contributor.filiacionTairum C. A.-
dc.contributor.filiacionTonoli C. C. C.-
dc.contributor.filiacionMurakami M. T.-
dc.contributor.filiacionOliveira M. A. de-
dc.contributor.filiacionNetto L. E. S.-
dc.rights.licenceLicencia Creative Commons Atribución (CC - By 4.0)es
dc.identifier.doi10.1016/j.freeradbiomed.2020.06.015-
Aparece en las colecciones: Publicaciones académicas y científicas - Facultad de Ciencias

Ficheros en este ítem:
Fichero Descripción Tamaño Formato   
10.1016j.freeradbiomed.2020.06.015.pdf3,6 MBAdobe PDFVisualizar/Abrir


Este ítem está sujeto a una licencia Creative Commons Licencia Creative Commons Creative Commons