Volume 234, 2022

A GPx-mimetic copper vanadate nanozyme mediates the release of nitric oxide from S-nitrosothiols

Abstract

Although reactive oxygen and nitrogen species (ROS/RNS), such as hydrogen peroxide (H2O2), nitric oxide (NO), hydroxyl radicals (OH˙), superoxide (O2) etc., play crucial roles in redox biology and cellular signaling, higher concentrations of these species lead to oxidative and nitrosative stress, which are associated with various pathophysiological conditions like neurodegeneration, cardiovascular diseases and cancer. There is growing evidence that functional impairment of the endothelium is one of the first recognizable signs of the development of atherosclerotic cardiovascular disease. A decreased bioavailability of NO and increased generation of ROS are the two major molecular changes associated with endothelial dysfunction. Therefore, it is a viable strategy to increase the bioavailability of NO while reducing the amount of ROS to prevent the progression of cardiovascular diseases. In this paper, we discuss for the first time that copper vanadate (CuV2O6) can not only release NO from S-nitrosothiols but can also control the ROS levels by functionally mimicking the antioxidant enzyme glutathione peroxidase (GPx) at physiological pH. We used several imaging techniques and spectroscopic measurements to understand the catalysis on the surface of the material during the reactions. The denitrosylation, as well as GPx-like activity, by CuV2O6 can be carried out multiple times without affecting the catalytic activity.

Graphical abstract: A GPx-mimetic copper vanadate nanozyme mediates the release of nitric oxide from S-nitrosothiols

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
04 अक्तूबर 2021
Accepted
06 दिसम्बर 2021
First published
09 दिसम्बर 2021

Faraday Discuss., 2022,234, 284-303

A GPx-mimetic copper vanadate nanozyme mediates the release of nitric oxide from S-nitrosothiols

S. Ghosh, P. Roy, S. Prasad and G. Mugesh, Faraday Discuss., 2022, 234, 284 DOI: 10.1039/D1FD00067E

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