| Literature DB >> 24288186 |
Dehui Zhang1, Igor Macinkovic, Nelmi O Devarie-Baez, Jia Pan, Chung-Min Park, Kate S Carroll, Milos R Filipovic, Ming Xian.
Abstract
Protein S-sulfhydration (forming -S-SH adducts from cysteine residues) is a newly defined oxidative posttranslational modification and plays an important role in H2 S-mediated signaling pathways. In this study we report the first selective, "tag-switch" method which can directly label protein S-sulfhydrated residues by forming stable thioether conjugates. Furthermore we demonstrate that H2 S alone cannot lead to S-sulfhydration and that the two possible physiological mechanisms include reaction with protein sulfenic acids (P-SOH) or the involvement of metal centers which would facilitate the oxidation of H2 S to HS(.) .Entities:
Keywords: hydrogen sulfide; protein S-sulfhydration; signal transduction; tag-switch; thiols
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Year: 2013 PMID: 24288186 PMCID: PMC4306352 DOI: 10.1002/anie.201305876
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336