Small-molecule modulation of cellular chaperones to treat protein misfolding disorders.

Lisa A Sloan, Martin C Fillmore, Ian Churcher
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Abstract

The correct folding of proteins is a fundamental process in the normal physiological functioning of cells, and is mediated by cellular chaperones including members of the Hsp70 family. Many diseases are caused by a failure of cellular chaperones to adequately maintain correct protein folding, and has led to the development of a therapeutic strategy to upregulate the activity of cellular chaperones in order to ameliorate intrinsic folding deficits. A large range of pharmacological agents that can induce cellular chaperones and correct deficits associated with misfolded proteins are known. This review surveys the mechanisms and compounds that have been used to modulate cellular chaperones, and discusses the continuing challenges in translating this approach into clinical improvements in the treatment of protein misfolding disorders.

小分子调节细胞伴侣治疗蛋白质错误折叠障碍。
蛋白质的正确折叠是细胞正常生理功能的一个基本过程,它是由包括Hsp70家族成员在内的细胞伴侣介导的。许多疾病是由于细胞伴侣蛋白未能充分维持正确的蛋白质折叠而引起的,这导致了一种治疗策略的发展,即上调细胞伴侣蛋白的活性,以改善内在的折叠缺陷。已知有大量的药物可以诱导细胞伴侣和纠正与错误折叠蛋白质相关的缺陷。本文综述了用于调节细胞伴侣蛋白的机制和化合物,并讨论了将这种方法转化为治疗蛋白质错误折叠疾病的临床改进所面临的持续挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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