Biochemistry · 2010 · 57 citations · 18 references
Natural SciencesBiochemistryChemistryCrystal StructureInorganic ChemistrySpectroscopyCrystallographyHeme Redox ChemistryPhotochemistryX-ray CrystallographyBinding Mode AnalysisHeme-ligand Redox InteractionsIron Redox ChemistryMyoglobin OxidationRadiation IntensitySingle Crystal AnalysisSingle-crystal CrystallographySynchrotron X-ray Spectroscopy
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.
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Ulrike B. Hendgen‐Cotta, Marc W. Merx, Sruti Shiva et al. · Proceedings of the National Academy of Sciences · 2008 · 417 citations · Full text
Haem-ligand switching during catalysis in crystals of a nitrogen-cycle enzyme
Pamela A. Williams, Vilmos Fülöp, Elspeth F. Garman et al. · Nature · 1997 · 292 citations