4.8 Article

Mechanism of Inactivation of Neuronal Nitric Oxide Synthase by (S)-2-Amino-5-(2-(methylthio)acetimidamido)pentanoic Acid

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 137, Issue 18, Pages 5980-5989

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.5b01202

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Funding

  1. National Institutes of Health [GM049725, GM057353]

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Nitric oxide synthase (NOS) catalysis the conversion of L-arginine to L-citrulline and the second messenger nitric oxide. Tlhree mechanistic pathways are proposed for the inactivation of,neuronal NOS (nNOS) by (S)-2-amino(2-(methylthio)acetimidamido)pentanoic acid (1): Sulfide oxidation, oxidative dethiolation, and oxidative demethylation. Four possible intermediates were synthesized. All compounds were assayed with nNOS, their IC50, K-I and k(inact) values were obtained, and their crystal structures were determined. The identification: and characterization of the products formed during inactivation provide evidence for the details of the inactivation mechanism. On the basis of these studies, the Most probable mechanism for the inactivation of nNOS involves oxidative demethylation with the resulting thiol coordinating to the cofactor heme iron. Although nNOS is a heme-containing enzyme, this is the first example of a NOS that catalyzes an S-demethylation reaction; the novel mechanism of inactivation described here could be applied to the design of inactivators of other heme-dependent enzymes.

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