Walker David T, Dassanayake Rohan S, Garcia Kamille A, Mukherjee Riya, Brasch Nicola E
Department of Chemistry and Biochemistry, Kent State University, Kent, OH 44242, USA.
Department of Chemistry and Biochemistry, Kent State University, Kent, OH 44242, USA ; School of Biomedical Sciences, Kent State University, Kent, OH 44242, USA.
Eur J Inorg Chem. 2013 Jun 1;2013(17). doi: 10.1002/ejic.201300254.
The essential but also toxic gaseous signaling molecule nitric oxide is scavenged by the reduced vitamin B complex cob(II)alamin. The resulting complex, nitroxylcobalamin (NO-Cbl(III)), is rapidly oxidized to nitrocobalamin (NOCbl) in the presence of oxygen; however it is unlikely that nitrocobalamin is itself stable in biological systems. Kinetic studies on the reaction between NOCbl and the important intracellular antioxidant, glutathione (GSH), are reported. In this study, a reaction pathway is proposed in which the β-axial ligand of NOCbl is first substituted by water to give aquacobalamin (HOCbl), which then reacts further with GSH to form glutathionylcobalamin (GSCbl). Independent measurements of the four associated rate constants k, k, k, and k support the proposed mechanism. These findings provide insight into the fundamental mechanism of ligand substitution reactions of cob(III)alamins with inorganic ligands at the β-axial site.
必需但又具有毒性的气态信号分子一氧化氮会被还原型复合维生素B钴胺素(cob(II)alamin)清除。生成的复合物硝酰钴胺素(NO-Cbl(III))在有氧存在的情况下会迅速氧化为硝基钴胺素(NOCbl);然而,硝基钴胺素本身在生物系统中不太可能稳定。本文报道了对NOCbl与重要的细胞内抗氧化剂谷胱甘肽(GSH)之间反应的动力学研究。在本研究中,提出了一种反应途径,其中NOCbl的β-轴向配体首先被水取代生成水合钴胺素(HOCbl),然后HOCbl再与GSH进一步反应形成谷胱甘肽钴胺素(GSCbl)。对四个相关速率常数k、k、k和k的独立测量支持了所提出的机制。这些发现为钴胺素(cob(III)alamin)在β-轴向位点与无机配体发生配体取代反应的基本机制提供了深入了解。