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新生蛋白质的错误折叠与聚集:体内镉毒性作用的一种新模式。

Misfolding and aggregation of nascent proteins: a novel mode of toxic cadmium action in vivo.

作者信息

Tamás Markus J, Fauvet Bruno, Christen Philipp, Goloubinoff Pierre

机构信息

Department of Chemistry and Molecular Biology, University of Gothenburg, 405 30, Gothenburg, Sweden.

Department of Plant Molecular Biology, Lausanne University, 1015, Lausanne, Switzerland.

出版信息

Curr Genet. 2018 Feb;64(1):177-181. doi: 10.1007/s00294-017-0748-x. Epub 2017 Sep 21.

Abstract

Cadmium is a highly poisonous metal and a human carcinogen, but the molecular mechanisms underlying its cellular toxicity are not fully understood. Recent findings in yeast cells indicate that cadmium exerts its deleterious effects by inducing widespread misfolding and aggregation of nascent proteins. Here, we discuss this novel mode of toxic heavy metal action and propose a mechanism by which molecular chaperones may reduce the damaging effects of heavy metal ions on protein structures.

摘要

镉是一种剧毒金属且是一种人类致癌物,但其细胞毒性背后的分子机制尚未完全明确。近期在酵母细胞中的研究发现表明,镉通过诱导新生蛋白质广泛的错误折叠和聚集来发挥其有害作用。在此,我们讨论这种有毒重金属作用的新模式,并提出一种分子伴侣可能减少重金属离子对蛋白质结构破坏作用的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45db/5778182/ec44b8b07bd4/294_2017_748_Fig1_HTML.jpg

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