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Characterization of Iron Dinitrosyl Species Formed in the Reaction of Nitric Oxide with a Biological Rieske Center

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dc.contributor Massachusetts Institute of Technology. Department of Chemistry
dc.contributor Lippard, Stephen J.
dc.contributor Tinberg, Christine E.
dc.contributor Tonzetich, Zachary J.
dc.contributor Do, Loi Hung
dc.contributor Lippard, Stephen J.
dc.creator Wang, Hongxin
dc.creator Yoda, Yoshitaka
dc.creator Cramer, Stephen P.
dc.creator Tinberg, Christine E.
dc.creator Tonzetich, Zachary J.
dc.creator Do, Loi Hung
dc.creator Lippard, Stephen J.
dc.date 2011-12-15T18:34:14Z
dc.date 2011-12-15T18:34:14Z
dc.date 2010-12
dc.date.accessioned 2023-03-01T18:10:19Z
dc.date.available 2023-03-01T18:10:19Z
dc.identifier 0002-7863
dc.identifier 1520-5126
dc.identifier http://hdl.handle.net/1721.1/67696
dc.identifier Tinberg, Christine E. et al. “Characterization of Iron Dinitrosyl Species Formed in the Reaction of Nitric Oxide with a Biological Rieske Center.” Journal of the American Chemical Society 132 (2010): 18168-18176. Web. 15 Dec. 2011. © 2011 American Chemical Society
dc.identifier https://orcid.org/0000-0002-2693-4982
dc.identifier.uri http://localhost:8080/xmlui/handle/CUHPOERS/279019
dc.description Reactions of nitric oxide with cysteine-ligated iron−sulfur cluster proteins typically result in disassembly of the iron−sulfur core and formation of dinitrosyl iron complexes (DNICs). Here we report the first evidence that DNICs also form in the reaction of NO with Rieske-type [2Fe-2S] clusters. Upon treatment of a Rieske protein, component C of toluene/o-xylene monooxygenase from Pseudomonas sp. OX1, with an excess of NO(g) or NO-generators S-nitroso-N-acetyl-d,l-pencillamine and diethylamine NONOate, the absorbance bands of the [2Fe-2S] cluster are extinguished and replaced by a new feature that slowly grows in at 367 nm. Analysis of the reaction products by electron paramagnetic resonance, Mössbauer, and nuclear resonance vibrational spectroscopy reveals that the primary product of the reaction is a thiolate-bridged diiron tetranitrosyl species, [Fe[subscript 2](μ-SCys)[subscript 2](NO)[subscript 4]], having a Roussin’s red ester (RRE) formula, and that mononuclear DNICs account for only a minor fraction of nitrosylated iron. Reduction of this RRE reaction product with sodium dithionite produces the one-electron-reduced RRE, having absorptions at 640 and 960 nm. These results demonstrate that NO reacts readily with a Rieske center in a protein and suggest that dinuclear RRE species, not mononuclear DNICs, may be the primary iron dinitrosyl species responsible for the pathological and physiological effects of nitric oxide in such systems in biology.
dc.description National Institute of General Medical Sciences (U.S.) (grant GM032134)
dc.description United States. Dept. of Energy (DOE OBER)
dc.description National Institute of General Medical Sciences (U.S.) (GM065440)
dc.description National Institutes of Health (U.S.). Biotechnology Training Fellowship (Grant T32 GM08334)
dc.description National Institute of General Medical Sciences (U.S.) (1 F32 GM082031-03)
dc.format application/pdf
dc.language en_US
dc.publisher American Chemical Society
dc.relation http://dx.doi.org/10.1021/ja106290p
dc.relation Journal of the American Chemical Society
dc.rights Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
dc.source Prof. Lippard via Erja Kajosalo
dc.title Characterization of Iron Dinitrosyl Species Formed in the Reaction of Nitric Oxide with a Biological Rieske Center
dc.type Article
dc.type http://purl.org/eprint/type/JournalArticle


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