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帕金蛋白调控丙酮酸激酶M2的活性。

Parkin Regulates the Activity of Pyruvate Kinase M2.

作者信息

Liu Kun, Li Fanzhou, Han Haichao, Chen Yue, Mao Zebin, Luo Jianyuan, Zhao Yingming, Zheng Bin, Gu Wei, Zhao Wenhui

机构信息

From the Department of Biochemistry and Molecular Biology, Peking University Health Science Center and Beijing Key Laboratory of Protein Posttranslational Modifications and Cell Function, Beijing 100191, China.

Ben May Department of Cancer Research, The University of Chicago, Chicago, Illinois 60637.

出版信息

J Biol Chem. 2016 May 6;291(19):10307-17. doi: 10.1074/jbc.M115.703066. Epub 2016 Mar 14.

Abstract

Parkin, a ubiquitin E3 ligase, is mutated in most cases of autosomal recessive early onset Parkinson disease. It was discovered that Parkin is also mutated in glioblastoma and other human malignancies and that it inhibits tumor cell growth. Here, we identified pyruvate kinase M2 (PKM2) as a unique substrate for parkin through biochemical purification. We found that parkin interacts with PKM2 both in vitro and in vivo, and this interaction dramatically increases during glucose starvation. Ubiquitylation of PKM2 by parkin does not affect its stability but decreases its enzymatic activity. Parkin regulates the glycolysis pathway and affects the cell metabolism. Our studies revealed the novel important roles of parkin in tumor cell metabolism and provided new insight for therapy of Parkinson disease.

摘要

帕金(Parkin)是一种泛素E3连接酶,在大多数常染色体隐性早发性帕金森病病例中发生突变。人们发现,帕金在胶质母细胞瘤和其他人类恶性肿瘤中也发生突变,并且它能抑制肿瘤细胞生长。在此,我们通过生化纯化确定丙酮酸激酶M2(PKM2)是帕金的一种独特底物。我们发现帕金在体外和体内均与PKM2相互作用,并且这种相互作用在葡萄糖饥饿期间显著增强。帕金对PKM2的泛素化不影响其稳定性,但会降低其酶活性。帕金调节糖酵解途径并影响细胞代谢。我们的研究揭示了帕金在肿瘤细胞代谢中的新的重要作用,并为帕金森病的治疗提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3708/4858978/dbe8d0e08c15/zbc0211643240001.jpg

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