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胆固醇作为共溶剂和膜蛋白的配体。

Cholesterol as a co-solvent and a ligand for membrane proteins.

机构信息

Department of Biochemistry, Center for Structural Biology and Institute of Chemical Biology, Vanderbilt University School of Medicine, Nashville, Tennessee, 37232.

出版信息

Protein Sci. 2014 Jan;23(1):1-22. doi: 10.1002/pro.2385. Epub 2013 Nov 18.

Abstract

As of mid 2013 a Medline search on "cholesterol" yielded over 200,000 hits, reflecting the prominence of this lipid in numerous aspects of animal cell biology and physiology under conditions of health and disease. Aberrations in cholesterol homeostasis underlie both a number of rare genetic disorders and contribute to common sporadic and complex disorders including heart disease, stroke, type II diabetes, and Alzheimer's disease. The corresponding author of this review and his lab stumbled only recently into the sprawling area of cholesterol research when they discovered that the amyloid precursor protein (APP) binds cholesterol, a topic covered by the Hans Neurath Award lecture at the 2013 Protein Society Meeting. Here, we first provide a brief overview of cholesterol-protein interactions and then offer our perspective on how and why binding of cholesterol to APP and its C99 domain (β-CTF) promotes the amyloidogenic pathway, which is closely related to the etiology of Alzheimer's disease.

摘要

截至 2013 年年中,在 Medline 上搜索“胆固醇”一词,得到了超过 20 万条结果,这反映了胆固醇在健康和疾病条件下动物细胞生物学和生理学的众多方面的重要性。胆固醇动态平衡的异常是许多罕见遗传疾病的基础,也是导致常见散发性和复杂疾病(包括心脏病、中风、II 型糖尿病和阿尔茨海默病)的原因之一。当他们发现淀粉样前体蛋白 (APP) 结合胆固醇时,本文的通讯作者及其实验室最近才涉足胆固醇研究的广泛领域,这是 2013 年蛋白质学会会议 Hans Neurath 奖演讲涵盖的主题。在这里,我们首先简要概述胆固醇-蛋白质相互作用,然后提供我们对 APP 和其 C99 结构域(β-CTF)与胆固醇结合如何以及为何促进淀粉样蛋白形成途径的看法,该途径与阿尔茨海默病的病因密切相关。

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