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Nitrosative Stress in the Nervous System: Guidelines for Designing Experimental Strategies to Study Protein S-Nitrosylation

机译:神经系统中的亚硝酸盐胁迫:设计研究蛋白质S-亚硝基化的实验策略的指南

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摘要

Reactive nitrogen species (RNS), such as nitric oxide (NO), exert their biological activity in large part through post-translational modification of cysteine residues, forming S-nitrosothiols. This chemical reaction proceeds via a process that we and our colleagues have termed protein S-nitrosylation. Under conditions of normal NO production, S-nitrosylation regulates the activity of many normal proteins. However, in degenerative conditions characterized by nitrosative stress, increased levels of NO lead to aberrant S-nitrosylation that contributes to the pathology of the disease. Thus, S-nitrosylation has been implicated in a wide range of cellular mechanisms, including mitochondrial function, proteostasis, transcriptional regulation, synaptic activity, and cell survival. In recent years, the research area of protein S-nitrosylation has become prominent due to improvements in the detection systems as well as the demonstration that protein S-nitrosylation plays a critical role in the pathogenesis of neurodegenerative and other neurological disorders. To further promote our understanding of how protein S-nitrosylation affects cellular systems, guidelines for the design and conduct of research on S-nitrosylated (or SNO-)proteins would be highly desirable, especially for those newly entering the field. In this review article, we provide a strategic overview of designing experimental approaches to study protein S-nitrosylation. We specifically focus on methods that can provide critical data to demonstrate that an S-nitrosylated protein plays a (patho-)physiologically-relevant role in a biological process. Hence, the implementation of the approaches described herein will contribute to further advancement of the study of S-nitrosylated proteins, not only in neuroscience but also in other research fields.
机译:一氧化氮(NO)等活性氮物质(RNS)在很大程度上通过半胱氨酸残基的翻译后修饰形成S-亚硝基硫醇,发挥其生物活性。这种化学反应是通过我们和我们的同事称为蛋白S-亚硝基化的过程进行的。在正常NO产生的条件下,S-亚硝基化调节许多正常蛋白质的活性。但是,在以亚硝化应激为特征的退化性疾病中,NO水平升高会导致S-亚硝基化异常,从而导致疾病的病理。因此,S-亚硝基化已涉及广泛的细胞机制,包括线粒体功能,蛋白稳态,转录调节,突触活性和细胞存活。近年来,由于检测系统的改进以及蛋白质S-亚硝基化在神经退行性疾病和其他神经系统疾病的发病机理中起着关键作用的证明,蛋白质S-亚硝基化的研究领域变得十分突出。为了进一步增进我们对蛋白质S-亚硝基化如何影响细胞系统的理解,非常需要用于设计和进行S-亚硝基化(或SNO-)蛋白质研究的指南,特别是对于那些刚进入该领域的科学家。在这篇评论文章中,我们提供了设计研究蛋白质S-亚硝基化的实验方法的战略概述。我们特别关注可以提供关键数据以证明S-亚硝基化蛋白在生物过程中起着(病理)生理相关作用的方法。因此,本文描述的方法的实施将不仅在神经科学领域而且在其他研究领域将有助于S-亚硝基化蛋白的研究的进一步发展。

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