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哺乳动物中含CHORD的蛋白melusin是一种与Hsp90和Sgt1相互作用的应激反应蛋白。

The mammalian CHORD-containing protein melusin is a stress response protein interacting with Hsp90 and Sgt1.

作者信息

Sbroggiò Mauro, Ferretti Roberta, Percivalle Elena, Gutkowska Malgorzata, Zylicz Alicja, Michowski Wojciech, Kuznicki Jacek, Accornero Federica, Pacchioni Beniamina, Lanfranchi Gerolamo, Hamm Jorg, Turco Emilia, Silengo Lorenzo, Tarone Guido, Brancaccio Mara

机构信息

Department of Genetics, Biology and Biochemistry, University of Torino, Molecular Biotechnology Center, via Nizza, 52, Torino, Italy.

出版信息

FEBS Lett. 2008 Jun 11;582(13):1788-94. doi: 10.1016/j.febslet.2008.04.058. Epub 2008 May 12.

Abstract

Melusin is a mammalian muscle specific CHORD containing protein capable of activating signal transduction pathways leading to cardiomyocytes hypertrophy in response to mechanical stress. To define melusin function we searched for molecular partners possibly involved in melusin dependent signal transduction. Here we show that melusin and heat shock proteins are co-regulated. Moreover, melusin directly binds to Hsp90, a ubiquitous chaperone involved in regulating several signaling pathways. In addition, melusin interacts with Sgt1, an Hsp90 binding molecule. Melusin does not behave as an Hsp90 substrate but rather as a chaperone capable to protect citrate synthase from heat induced aggregation. These results describe melusin as a new component of the Hsp90 chaperone machinery.

摘要

肌联蛋白是一种哺乳动物肌肉特异性含CHORD结构域的蛋白质,能够激活信号转导通路,使心肌细胞在机械应力作用下发生肥大。为了明确肌联蛋白的功能,我们寻找了可能参与肌联蛋白依赖性信号转导的分子伴侣。在此我们发现肌联蛋白与热休克蛋白共同调节。此外,肌联蛋白直接与Hsp90结合,Hsp90是一种参与调节多种信号通路的普遍存在的伴侣蛋白。另外,肌联蛋白与Sgt1相互作用,Sgt1是一种Hsp90结合分子。肌联蛋白并非作为Hsp90的底物发挥作用,而是作为一种伴侣蛋白,能够保护柠檬酸合酶免受热诱导的聚集。这些结果表明肌联蛋白是Hsp90伴侣蛋白机制的一个新组分。

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