Unknown

Dataset Information

0

Heme-assisted S-nitrosation desensitizes ferric soluble guanylate cyclase to nitric oxide.


ABSTRACT: Nitric oxide (NO) signaling regulates key processes in cardiovascular physiology, specifically vasodilation, platelet aggregation, and leukocyte rolling. Soluble guanylate cyclase (sGC), the mammalian NO sensor, transduces an NO signal into the classical second messenger cyclic GMP (cGMP). NO binds to the ferrous (Fe(2+)) oxidation state of the sGC heme cofactor and stimulates formation of cGMP several hundred-fold. Oxidation of the sGC heme to the ferric (Fe(3+)) state desensitizes the enzyme to NO. The heme-oxidized state of sGC has emerged as a potential therapeutic target in the treatment of cardiovascular disease. Here, we investigate the molecular mechanism of NO desensitization and find that sGC undergoes a reductive nitrosylation reaction that is coupled to the S-nitrosation of sGC cysteines. We further characterize the kinetics of NO desensitization and find that heme-assisted nitrosothiol formation of ?1Cys-78 and ?1Cys-122 causes the NO desensitization of ferric sGC. Finally, we provide evidence that the mechanism of reductive nitrosylation is gated by a conformational change of the protein. These results yield insights into the function and dysfunction of sGC in cardiovascular disease.

SUBMITTER: Fernhoff NB 

PROVIDER: S-EPMC3522300 | biostudies-literature | 2012 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Heme-assisted S-nitrosation desensitizes ferric soluble guanylate cyclase to nitric oxide.

Fernhoff Nathaniel B NB   Derbyshire Emily R ER   Underbakke Eric S ES   Marletta Michael A MA  

The Journal of biological chemistry 20121023 51


Nitric oxide (NO) signaling regulates key processes in cardiovascular physiology, specifically vasodilation, platelet aggregation, and leukocyte rolling. Soluble guanylate cyclase (sGC), the mammalian NO sensor, transduces an NO signal into the classical second messenger cyclic GMP (cGMP). NO binds to the ferrous (Fe(2+)) oxidation state of the sGC heme cofactor and stimulates formation of cGMP several hundred-fold. Oxidation of the sGC heme to the ferric (Fe(3+)) state desensitizes the enzyme t  ...[more]

Similar Datasets

| S-EPMC4001857 | biostudies-literature
| S-EPMC8640258 | biostudies-literature
| S-EPMC305806 | biostudies-literature
2014-06-19 | GSE48099 | GEO
| S-EPMC2791033 | biostudies-literature
| S-EPMC5066868 | biostudies-literature
| S-EPMC4932850 | biostudies-literature
2014-06-19 | E-GEOD-48099 | biostudies-arrayexpress
| S-EPMC545542 | biostudies-literature
| S-EPMC1201615 | biostudies-literature