Biochemical characterization of yeast mitochondrial Grx5 monothiol glutaredoxin
dc.contributor.author | Tamarit Sumalla, Jordi | |
dc.contributor.author | Bellí i Martínez, Gemma | |
dc.contributor.author | Cabiscol Català, Elisa | |
dc.contributor.author | Herrero Perpiñán, Enrique | |
dc.contributor.author | Ros Salvador, Joaquim | |
dc.date.accessioned | 2015-07-02T09:26:36Z | |
dc.date.issued | 2003 | |
dc.description.abstract | Grx5 is a yeast mitochondrial protein involved in iron- sulfur biogenesis that belongs to a recently described family of monothiolic glutaredoxin-like proteins. No member of this family has been biochemically charac- terized previously. Grx5 contains a conserved cysteine residue (Cys-60) and a non-conserved one (Cys-117). In this work, we have purified wild type and mutant C60S and C117S proteins and characterized their biochemical properties. A redox potential of ؊175 mV was calculated for wild type Grx5. The pKa values obtained by titration of mutant proteins with iodoacetamide at different pHs were 5.0 for Cys-60 and 8.2 for Cys-117. When Grx5 was incubated with glutathione disulfide, a transient mixed disulfide was formed between glutathione and the cys- tein 60 of the protein because of its low pKa. Binding of glutathione to Cys-60 promoted a decrease in the Cys- 117 pKa value that triggered the formation of a disulfide bond between both cysteine residues of the protein, in- dicating that Cys-117 plays an essential role in the cat- alytic mechanism of Grx5. The disulfide bond in Grx5 could be reduced by GSH but at a rate at least 20 times slower than that observed for the reduction of glutare- doxin 1 from E. coli, a dithiolic glutaredoxin. This slow reduction rate could suggest that GSH may not be the physiologic reducing agent of Grx5. The fact that wild type Grx5 efficiently reduced a glutathiolated protein used as a substrate indicated that Grx5 may act as a thiol reductase inside the mitochondria. | ca_ES |
dc.identifier.doi | https://doi.org/10.1074/jbc.M303477200 | |
dc.identifier.idgrec | 000005 | |
dc.identifier.issn | 0021-9258 | |
dc.identifier.uri | http://hdl.handle.net/10459.1/48398 | |
dc.language.iso | eng | ca_ES |
dc.publisher | The American Society for Biochemistry and Molecular Biology | ca_ES |
dc.relation.isformatof | Reproducció del document publicat a https://doi.org/10.1074/jbc.M303477200 | ca_ES |
dc.relation.ispartof | The Journal of Biological Chemistry, 2003, vol. 278, núm 28, p. 25745-25751 | ca_ES |
dc.rights | (c) The American Society for Biochemistry and Molecular Biology, 2003 | ca_ES |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | ca_ES |
dc.title | Biochemical characterization of yeast mitochondrial Grx5 monothiol glutaredoxin | ca_ES |
dc.type | article | ca_ES |
dc.type.version | publishedVersion | ca_ES |
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