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pubmed-article:21204537pubmed:abstractTextCORM-3, [fac-Ru(CO)(3)Cl(?(2)-H(2)NCH(2)CO(2))], is a well-known carbon monoxide releasing molecule (CORM) capable of delivering CO in vivo. Herein we show for the first time that the interactions of CORM-3 with proteins result in the loss of a chloride ion, glycinate, and one CO ligand. The rapid formation of stable adducts between the protein and the remaining cis-Ru(II)(CO)(2) fragments was confirmed by Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES), Liquid-Chromatography Mass Spectrometry (LC-MS), Infrared Spectroscopy (IR), and X-ray crystallography. Three Ru coordination sites are observed in the structure of hen egg white lysozyme crystals soaked with CORM-3. The site with highest Ru occupancy (80%) shows a fac-[(His15)Ru(CO)(2)(H(2)O)(3)] structure.lld:pubmed
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pubmed-article:21204537pubmed:authorpubmed-author:RomãoCarlos...lld:pubmed
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pubmed-article:21204537pubmed:authorpubmed-author:SeixasJoão...lld:pubmed
pubmed-article:21204537pubmed:authorpubmed-author:MukhopadhyayA...lld:pubmed
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pubmed-article:21204537pubmed:articleTitleCORM-3 reactivity toward proteins: the crystal structure of a Ru(II) dicarbonyl-lysozyme complex.lld:pubmed
pubmed-article:21204537pubmed:affiliationREQUIMTE-CQFB, Departamento de Qui?mica, FCT-UNL, 2829-516 Caparica, Portugal.lld:pubmed
pubmed-article:21204537pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21204537pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed