| Literature DB >> 20568729 |
Jun Yi1, Allen M Orville, John M Skinner, Michael J Skinner, George B Richter-Addo.
Abstract
Exposure of a single crystal of the nitrite adduct of ferric myoglobin (Mb) at 100 K to high-intensity synchrotron X-ray radiation resulted in changes in the UV-vis spectrum that can be attributed to reduction of the ferric compound to the ferrous derivative. We employed correlated single-crystal spectroscopy with crystallography to further characterize this photoproduct. The 1.55 A resolution crystal structure of the photoproduct reveals retention of the O-binding mode for binding of nitrite to the iron center. The data are consistent with cryogenic generation and trapping, at 100 K, of a ferrous d(6) Mb(II)(ONO)* complex by photoreduction of the ferric precursor crystals using high-intensity X-ray radiation.Entities:
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Year: 2010 PMID: 20568729 PMCID: PMC2916933 DOI: 10.1021/bi100801g
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162