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亚硝基硫醇形成与降解的生物学机制:亚硝基化的特异性是如何实现的?

Biological Mechanisms of -Nitrosothiol Formation and Degradation: How Is Specificity of -Nitrosylation Achieved?

作者信息

Massa Christopher M, Liu Ziping, Taylor Sheryse, Pettit Ashley P, Stakheyeva Marena N, Korotkova Elena, Popova Valentina, Atochina-Vasserman Elena N, Gow Andrew J

机构信息

Department of Pharmacology & Toxicology, Ernest Mario School of Pharmacy, Rutgers University, Piscataway, NJ 08848, USA.

RASA Center in Tomsk, Tomsk Polytechnic University, 634050 Tomsk, Russia.

出版信息

Antioxidants (Basel). 2021 Jul 12;10(7):1111. doi: 10.3390/antiox10071111.

Abstract

The modification of protein cysteine residues underlies some of the diverse biological functions of nitric oxide (NO) in physiology and disease. The formation of stable nitrosothiols occurs under biologically relevant conditions and time scales. However, the factors that determine the selective nature of this modification remain poorly understood, making it difficult to predict thiol targets and thus construct informatics networks. In this review, the biological chemistry of NO will be considered within the context of nitrosothiol formation and degradation whilst considering how specificity is achieved in this important post-translational modification. Since nitrosothiol formation requires a formal one-electron oxidation, a classification of reaction mechanisms is proposed regarding which species undergoes electron abstraction: NO, thiol or S-NO radical intermediate. Relevant kinetic, thermodynamic and mechanistic considerations will be examined and the impact of sources of NO and the chemical nature of potential reaction targets is also discussed.

摘要

蛋白质半胱氨酸残基的修饰是一氧化氮(NO)在生理和疾病中多种生物学功能的基础。稳定的亚硝基硫醇的形成发生在生物学相关的条件和时间尺度下。然而,决定这种修饰选择性的因素仍知之甚少,这使得预测硫醇靶点并构建信息网络变得困难。在这篇综述中,将在亚硝基硫醇形成和降解的背景下考虑NO的生物化学,同时考虑在这一重要的翻译后修饰中如何实现特异性。由于亚硝基硫醇的形成需要形式上的单电子氧化,因此提出了关于哪种物种经历电子提取的反应机制分类:NO、硫醇或S-NO自由基中间体。将研究相关的动力学、热力学和机理方面的考虑因素,并讨论NO来源的影响以及潜在反应靶点的化学性质。

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