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蛋白质S-亚硝基化在中枢神经系统疾病线粒体质量控制中的作用

The Role of Protein S-Nitrosylation in Mitochondrial Quality Control in Central Nervous System Diseases.

作者信息

Qiu Fang, Liu Yuqiang, Liu Zhiheng

机构信息

Department of Burn and Plastic Surgery, Shenzhen Longhua District Central Hospital, Shenzhen, Guangdong, China.

Department of Anesthesiology, Shenzhen Second People's Hospital, the First Affiliated Hospital of Shenzhen University, Shenzhen, China.

出版信息

Aging Dis. 2024 Mar 25;16(5):2641-2658. doi: 10.14336/AD.2024.0099.

Abstract

S-Nitrosylation is a reversible covalent post-translational modification. Under physiological conditions, S-nitrosylation plays a dynamic role in a wide range of biological processes by regulating the function of substrate proteins. Like other post-translational modifications, S-nitrosylation can affect protein conformation, activity, localization, aggregation, and protein interactions. Aberrant S-nitrosylation can lead to protein misfolding, mitochondrial fragmentation, synaptic damage, and autophagy. Mitochondria are essential organelles in energy production, metabolite biosynthesis, cell death, and immune responses, among other processes. Mitochondrial dysfunction can result in cell death and has been implicated in the development of many human diseases. Recent evidence suggests that S-nitrosylation and mitochondrial dysfunction are important modulators of the progression of several diseases. In this review, we highlight recent findings regarding the aberrant S- nitrosylation of mitochondrial proteins that regulate mitochondrial biosynthesis, fission and fusion, and autophagy. Specifically, we discuss the mechanisms by which S-nitrosylated mitochondrial proteins exercise mitochondrial quality control under pathological conditions, thereby influencing disease. A better understanding of these pathological events may provide novel therapeutic targets to mitigate the development of neurological diseases.

摘要

S-亚硝基化是一种可逆的共价翻译后修饰。在生理条件下,S-亚硝基化通过调节底物蛋白的功能,在广泛的生物过程中发挥动态作用。与其他翻译后修饰一样,S-亚硝基化可影响蛋白质的构象、活性、定位、聚集及蛋白质相互作用。异常的S-亚硝基化可导致蛋白质错误折叠、线粒体碎片化、突触损伤及自噬。线粒体是能量产生、代谢物生物合成、细胞死亡及免疫反应等众多过程中必不可少的细胞器。线粒体功能障碍可导致细胞死亡,并与多种人类疾病的发生发展有关。最近的证据表明,S-亚硝基化和线粒体功能障碍是多种疾病进展的重要调节因子。在本综述中,我们重点介绍了有关调节线粒体生物合成、分裂与融合及自噬的线粒体蛋白异常S-亚硝基化的最新研究结果。具体而言,我们讨论了S-亚硝基化的线粒体蛋白在病理条件下行使线粒体质量控制从而影响疾病的机制。更好地理解这些病理事件可能为减轻神经疾病的发展提供新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fdd/12339124/140e0ad1f5b9/AD-16-5-2641-g1.jpg

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