Protein S-sulfhydration as a major sources of H2S bioactivity

Guangdong Yang
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引用次数: 8

Abstract

The physiological and biomedical importance of hydrogen sulfide (H 2 S) has been extensively studied in our body.  H 2 S can be endogenously produced in a variety of cells and tissues by cystathionine γ-lyase, cystathionine β-synthase, and/or 3-mercaptopyruvate sulfurtransferase, and is involved in the regulation of vascular function, cell growth, insulin secretion, neurotransmission, myocardial contractility, inflammation, and nociception, etc.  H 2 S post-translationally modifies proteins by yielding a hydropersulfide moiety (–SSH) in specific cysteine residue(s), termed as S -sulfhydration.  It is becoming increasingly recognized that S -sulfhydration is a major sources of H 2 S bioactivity.  In this research highlight, we discuss our latest published findings which demonstrate the S -sulfhydration regulation of proteins by H 2 S and their importance in aging and cancer protection.
蛋白质s -巯基化是硫化氢生物活性的主要来源
硫化氢(h2s)的生理和生物医学重要性已经在我们体内得到了广泛的研究。h2s可通过半胱硫氨酸γ-裂解酶、半胱硫氨酸β-合酶和/或3-巯基丙酮酸硫转移酶在多种细胞和组织中内源性产生,参与血管功能、细胞生长、胰岛素分泌、神经传递、心肌收缩、炎症和伤害感受等调节。h2s翻译后通过在特定的半胱氨酸残基(S)中产生氢过硫化物片段(-SSH)修饰蛋白质,称为S -巯基化。越来越多的人认识到S -硫酸化是h2s生物活性的主要来源。在本研究重点中,我们讨论了我们最新发表的研究结果,证明了S -巯基化对蛋白质的调节及其在衰老和癌症保护中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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