Mechanistic Studies on the Reaction of Nitrocobalamin with Glutathione: Kinetic Evidence for Formation of an Aquacobalamin Intermediate

被引:9
|
作者
Walker, David T. [1 ]
Dassanayake, Rohan S. [1 ]
Garcia, Kamille A. [1 ]
Mukherjee, Riya [1 ]
Brasch, Nicola E. [1 ,2 ]
机构
[1] Kent State Univ, Dept Chem & Biochem, Kent, OH 44242 USA
[2] Kent State Univ, Sch Biomed Sci, Kent, OH 44242 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Vitamin B12; Cob(III)alamin; Bioinorganic chemistry; Kinetics; Reaction mechanisms; LIGAND-SUBSTITUTION-REACTIONS; NITRIC-OXIDE; METHIONINE SYNTHASE; SPECTROSCOPIC EVIDENCE; SPINAL-CORD; COBALAMIN; VITAMIN-B-12; HYDROXOCOBALAMIN; BINDING; INACTIVATION;
D O I
10.1002/ejic.201300254
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The essential but also toxic gaseous signaling molecule nitric oxide is scavenged by the reduced vitamin B12 complex cob(II)alamin. The resulting complex, nitroxylcobalamin [NO--Cbl(III)], is rapidly oxidized to nitrocobalamin (NO2Cbl) in the presence of oxygen; however, it is unlikely that nitrocobalamin is itself stable in biological systems. Kinetic studies on the reaction between NO2Cbl and the important intracellular antioxidant, glutathione (GSH), are reported. In this study, a reaction pathway is proposed in which the -axial ligand of NO2Cbl is first substituted by water to give aquacobalamin (H2OCbl+), which then reacts further with GSH to form glutathionylcobalamin (GSCbl). Independent measurements of the four associated rate constants k1, k-1, k2, and k-2 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 -axial site.
引用
收藏
页码:3049 / 3053
页数:5
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