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Modeling Selenoprotein Se -Nitrosation: Synthesis of a Se -Nitrososelenocysteine with Persistent Stability.

Ryosuke MasudaSatoru KuwanoKei Goto
Published in: Journal of the American Chemical Society (2023)
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 1 H and 77 Se 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.
Keyphrases
  • room temperature
  • magnetic resonance
  • small molecule
  • high resolution
  • single molecule
  • hydrogen peroxide
  • computed tomography
  • mass spectrometry
  • genetic diversity