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J Am Chem Soc ; 145(26): 14184-14189, 2023 07 05.
Artículo en Inglés | MEDLINE | ID: mdl-37267591

RESUMEN

The Se-nitrosation in selenoproteins such as glutathione peroxidase and thioredoxin reductase to produce Se-nitrososelenocysteines (Sec-SeNOs) has been proposed to play crucial roles in signaling processes mediated by reactive nitrogen species and nitrosative-stress responses, although chemical evidence for the formation of Sec-SeNOs has been elusive not only in proteins but also in small-molecule systems. Herein, we report the first synthesis of a Sec-SeNO by employing a selenocysteine model system that bears a protective molecular cradle. The Sec-SeNO was characterized using 1H and 77Se nuclear magnetic resonance as well as ultraviolet/visible spectroscopy and found to have persistent stability at room temperature in solution. The reaction processes involving the Sec-SeNO provide experimental information that serves as a chemical basis for elucidating the reaction mechanisms involving the SeNO species in biological functions, as well as in selenol-catalyzed NO generation from S-nitrosothiols.


Asunto(s)
Selenio , Selenoproteínas , Nitrosación , Selenoproteínas/metabolismo , Glutatión Peroxidasa/metabolismo , Reductasa de Tiorredoxina-Disulfuro/metabolismo , Selenocisteína/química , Selenio/metabolismo
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