Oxidation and loss of heme in soluble guanylyl cyclase from Manduca sexta |
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Authors: | Fritz Bradley G Hu Xiaohui Brailey Jacqueline L Berry Robert E Walker F Ann Montfort William R |
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Affiliation: | Department of Chemistry and Biochemistry, University of Arizona, Tucson, Arizona 85721, United States. |
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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. |
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