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dc.creatorLopez-Sanchez, L.M. (Laura M.)-
dc.creatorCorrales, F.J. (Fernando José)-
dc.creatorMata, M. (Manuel) de la-
dc.creatorMuntane, J. (Jordi)-
dc.creatorRodriguez-Ariza, A. (Antonio)-
dc.date.accessioned2012-04-02T07:51:11Z-
dc.date.available2012-04-02T07:51:11Z-
dc.date.issued2008-
dc.identifier.citationLopez-Sanchez LM, Corrales FJ, De La Mata M, Muntane J, Rodriguez-Ariza A. Detection and proteomic identification of S-nitrosated proteins in human hepatocytes. Methods Enzymol 2008;440:273-281.es_ES
dc.identifier.issn1557-7988-
dc.identifier.urihttps://hdl.handle.net/10171/21484-
dc.description.abstractThe S-nitrosation of protein thiols is a redox-based posttranslational modification that modulates protein function and cell phenotype. Although the detection of S-nitrosated proteins is problematical because of the lability of S-nitrosothiols, an increasing range of proteins has been shown to undergo S-nitrosation with the improvement of molecular tools. This chapter describes the methodology used to identify potential targets of S-nitrosation in cultured primary human hepatocytes using proteomic approaches. This methodology is based on the biotin switch method, which labels S-nitrosated proteins with an affinity tag, allowing their selective detection and proteomic identification.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/closedAccess-
dc.subjectHepatocytes/metabolismes_ES
dc.subjectProteins/analysises_ES
dc.subjectProteins/metabolismes_ES
dc.subjectProteomics/methodses_ES
dc.subjectS-Nitrosothiols/analysises_ES
dc.subjectS-Nitrosothiols/metabolismes_ES
dc.titleDetection and proteomic identification of S-nitrosated proteins in human hepatocyteses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S0076687907008178es_ES
dc.type.driverinfo:eu-repo/semantics/articlees_ES

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