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Mechanisms of biological S-nitrosation and its measurement.

机译:生物S-亚硝化的机理及其测量。

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摘要

Nitric oxide (NO) exhibits multiple biological actions through formation of various oxidized intermediates derived from NO. Among them, nitrosothiol adducts (RS-NOs) with the sulfhydryl moiety of proteins and amino acids appears to be an important species in view of its unique chemical reactivity. Understanding of the biologically relevant S-nitrosation mechanism is essential because RS-NOs seem to be critically involved in modulation of intracellular and intercellular signal transduction, including gene transcription, cell apoptosis, and oxidative stress. RS-NOs have been recently found to be formed efficiently via one-electron oxidation of NO catalyzed by ceruloplasmin, a major copper-containing protein in mammalian plasma. Ceruloplasmin is synthesized mainly by hepatocytes, but it is also expressed by other cells such as macrophages and astrocytes. Once RS-NOs are formed, they function as NO transporters in biological systems, the NO being transferred to different sulfhydryls of various biomolecules. This transfer may be mediated by transnitrosation reactions occurring chemically or enzymatically by a means of specific enzymes such as protein disulfide isomerase. The molecular mechanism of biological S-nitrosation is discussed as related to the important physiological and pathophysiological functions of RS-NOs. Also, RS-NO assays that are being successfully used for detection of biological S-nitrosation are briefly reviewed.
机译:一氧化氮(NO)通过形成多种源自NO的氧化中间体而表现出多种生物学作用。其中,考虑到其独特的化学反应性,具有蛋白质和氨基酸巯基部分的亚硝基硫醇加合物(RS-NOs)似乎是重要的物种。了解生物学相关的S-亚硝化机制至关重要,因为RS-NOs似乎与细胞内和细胞间信号转导的调控密切相关,包括基因转录,细胞凋亡和氧化应激。最近发现RS-NOs是通过铜蓝蛋白催化的NO的单电子氧化而有效形成的。铜蓝蛋白是哺乳动物血浆中一种主要的含铜蛋白。铜蓝蛋白主要由肝细胞合成,但也可由其他细胞如巨噬细胞和星形胶质细胞表达。 RS-NO形成后,便会在生物系统中充当NO转运蛋白,将NO转移到各种生物分子的不同巯基上。该转移可以通过转氨作用通过化学或酶促发生的亚硝化反应来介导,所述亚硝化反应是通过特定的酶如蛋白质二硫键异构酶发生的。讨论了生物S-亚硝化的分子机理,与RS-NOs的重要生理和病理生理功能有关。此外,简要回顾了已成功用于生物S-亚硝化检测的RS-NO分析。

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