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帕金蛋白的S-亚硝基化作用调控泛素化过程,并损害帕金蛋白的保护功能。

S-nitrosylation of parkin regulates ubiquitination and compromises parkin's protective function.

作者信息

Chung Kenny K K, Thomas Bobby, Li Xiaojie, Pletnikova Olga, Troncoso Juan C, Marsh Laura, Dawson Valina L, Dawson Ted M

机构信息

Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

出版信息

Science. 2004 May 28;304(5675):1328-31. doi: 10.1126/science.1093891. Epub 2004 Apr 22.

Abstract

Parkin is an E3 ubiquitin ligase involved in the ubiquitination of proteins that are important in the survival of dopamine neurons in Parkinson's disease (PD). We show that parkin is S-nitrosylated in vitro, as well as in vivo in a mouse model of PD and in brains of patients with PD and diffuse Lewy body disease. Moreover, S-nitrosylation inhibits parkin's ubiquitin E3 ligase activity and its protective function. The inhibition of parkin's ubiquitin E3 ligase activity by S-nitrosylation could contribute to the degenerative process in these disorders by impairing the ubiquitination of parkin substrates.

摘要

帕金蛋白是一种E3泛素连接酶,参与对帕金森病(PD)中多巴胺能神经元存活至关重要的蛋白质的泛素化过程。我们发现,帕金蛋白在体外以及在帕金森病小鼠模型、帕金森病和弥漫性路易体病患者的大脑中均发生了S-亚硝基化。此外,S-亚硝基化抑制了帕金蛋白的泛素E3连接酶活性及其保护功能。S-亚硝基化对帕金蛋白泛素E3连接酶活性的抑制可能通过损害帕金蛋白底物的泛素化而导致这些疾病中的退行性过程。

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