期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 290, 期 45, 页码 26866-26880出版社
ELSEVIER
DOI: 10.1074/jbc.M115.672816
关键词
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资金
- Comision Sectorial de Investigacion Cientifica (Universidad de la Republica)
- L'Oreal-UNESCO, Uruguay
- Friedrich-Alexander University of Erlangen-Nuremberg (MRIC)
- Agencia Nacional de Investigacion e Innovacion
- PEDECIBA, Uruguay
Background: Hydrogen sulfide (H2S) modulates physiological processes in mammals. Results: The reactivity of H2S toward disulfides (RSSR) and albumin sulfenic acid (RSOH) to form persulfides (RSSH) was assessed. Conclusion: H2S is less reactive than thiols. Persulfides have enhanced nucleophilicity. Significance: This kinetic study helps rationalize the contribution of the reactions with oxidized thiol derivatives to H2S biology.
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