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Reduction of sulfenic acids by ascorbate in proteins, connecting thiol-dependent to alternative redox pathways

dc.contributor.authorAnschau, Valesca
dc.contributor.authorFerrer-Sueta, Gerardo
dc.contributor.authorAleixo-Silva, Rogerio Luis
dc.contributor.authorBannitz Fernandes, Renata
dc.contributor.authorTairum, Carlos A.
dc.contributor.authorTonoli, Celisa Caldana Costa
dc.contributor.authorMurakami, Mario Tyago
dc.contributor.authorde Oliveira, Marcos Antonio [UNESP]
dc.contributor.authorNetto, Luis Eduardo Soares
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidad de La República
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionNational Center for Research in Energy and Materials
dc.date.accessioned2020-12-12T02:15:36Z
dc.date.available2020-12-12T02:15:36Z
dc.date.issued2020-08-20
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 kcat/KMAsc 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.en
dc.description.affiliationDepartamento de Genética e Biologia Evolutiva Instituto de Biociências Universidade de São Paulo
dc.description.affiliationLaboratorio de Fisicoquímica Biológica Instituto de Química Biológica Facultad de Ciencias Universidad de La República, Iguá 4225
dc.description.affiliationCentro de Investigaciones Biomédicas (CEINBIO) Universidad de La República
dc.description.affiliationInstituto de Biociências UNESP Campus Do Litoral Paulista, São Vicente
dc.description.affiliationBrazilian Biorenewables National Laboratory National Center for Research in Energy and Materials
dc.description.affiliationUnespInstituto de Biociências UNESP Campus Do Litoral Paulista, São Vicente
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipUniversidad de la República Uruguay
dc.description.sponsorshipIdFAPESP: 2013/07937-8
dc.description.sponsorshipIdUniversidad de la República Uruguay: 54/2013
dc.format.extent207-216
dc.identifierhttp://dx.doi.org/10.1016/j.freeradbiomed.2020.06.015
dc.identifier.citationFree Radical Biology and Medicine, v. 156, p. 207-216.
dc.identifier.doi10.1016/j.freeradbiomed.2020.06.015
dc.identifier.issn1873-4596
dc.identifier.issn0891-5849
dc.identifier.scopus2-s2.0-85088112238
dc.identifier.urihttp://hdl.handle.net/11449/200769
dc.language.isoeng
dc.relation.ispartofFree Radical Biology and Medicine
dc.sourceScopus
dc.subjectAscorbate
dc.subjectPeroxides
dc.subjectPeroxiredoxin
dc.subjectSulfenic acid
dc.titleReduction of sulfenic acids by ascorbate in proteins, connecting thiol-dependent to alternative redox pathwaysen
dc.typeArtigo
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, São Vicentept
unesp.departmentCiências Biológicas - IBCLPpt

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