| Literature DB >> 21639146 |
Bradley G Fritz1, Xiaohui Hu, Jacqueline L Brailey, Robert E Berry, F Ann Walker, William R Montfort.
Abstract
Oxidation and loss of heme in soluble guanylyl/guanylate cyclase (sGC), the nitric oxide receptor, is thought to be a major contributor to cardiovascular disease and is the target of compounds BAY 58-2667 and HMR1766. Using spectroelectrochemical titration, we found a truncated sGC to be highly stable in the ferrous state (234 mV) and to bind ferrous heme tightly even in the presence of NO, despite the NO-induced release of the proximal histidine. In contrast, oxidized sGC readily loses ferric heme to myoglobin (0.47 ± 0.02 h(-1)). Peroxynitrite, the presumed cellular oxidant, readily oxidizes sGC in 5 mM glutathione.Entities:
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Year: 2011 PMID: 21639146 PMCID: PMC3128461 DOI: 10.1021/bi200794c
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162