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Research Articles

Reactions of glutathionylcobalamin with nitroxyl and its donor, Angeli’s salt

ORCID Icon, , , ORCID Icon, &
Pages 682-696 | Received 30 Aug 2023, Accepted 21 Dec 2023, Published online: 08 Feb 2024
 

Abstract

We investigated the reaction between glutathionylcobalamin (GSCbl), a tight complex of cobalamin with glutathione (GSH), and nitroxyl (HNO) produced upon decomposition of Angeli’s salt using ultraviolet-visible spectroscopy and 1H NMR. The reaction in neutral and alkaline media leads to formation of nitrosylcobalamin (NOCbl). Simulation of the kinetic traces using the ChemMech program package suggested that the mechanism of the process involves complexation between HNO and GSCbl and further decomposition of the complex into the products. The complex participates in an acid-base equilibrium (pKa = 8.9), and the deprotonated form decomposes to NOCbl more rapidly than the protonated species. At pH 7.4, the reaction of HNO with GSCbl proceeds ca.103-times more slowly than with free GSH. GSCbl can react directly with the monoprotonated anion of Angeli’s salt (HN2O3) to produce nitrocobalamin (NO2Cbl). The reaction between GSCbl and HN2O3 is insignificant in an alkaline medium and is accelerated upon acidification of the medium. The critical step of the process is the complexation between GSCbl and HN2O3. The produced complex is involved in an acid-base equilibrium (pKa = 8.1): the protonated form can be transformed to NO2Cbl and GSNHO, whereas the deprotonated species decompose to initial reactants.

Disclosure statement

The authors declare no competing financial interests.

Additional information

Funding

This work was supported by the Russian Science Foundation (project no. 21-73-10057) to IAD. The study was carried out using the resources of the Center for Shared Use of Scientific Equipment of the ISUCT (with the support of the Ministry of Science and Higher Education of Russia, grant No. 075-15-2021-671) and equipment of the Shared Facility Center of the Upper Volga Regional Center of Physicochemical Studies.

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