Luheshi Leila M, Crowther Damian C, Dobson Christopher M
Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK.
Curr Opin Chem Biol. 2008 Feb;12(1):25-31. doi: 10.1016/j.cbpa.2008.02.011. Epub 2008 Mar 18.
Protein misfolding is the underlying cause of many highly debilitating disorders ranging from Alzheimer's Disease to Cystic Fibrosis. Great strides have been made recently in understanding what causes proteins to misfold, primarily through the use of biophysical and computational techniques that enable systematic and quantitative analysis of the effects of a range of different perturbations in proteins. Correlation of the results of such analyses with observations made in animal models of disease has however been limited by their seemingly irreconcilable differences in methodology and scope. Several recent studies have however begun to overcome this limitation by combining the two approaches. This strategy has made it possible to investigate many of the consequences of protein misfolding in vivo, ranging from disease pathogenesis to epigenetic regulation, in the context of the fundamental physico-chemical principles derived from extensive and highly detailed studies undertaken in vitro.
蛋白质错误折叠是许多严重致残性疾病的根本原因,从阿尔茨海默病到囊性纤维化。最近在理解蛋白质错误折叠的原因方面取得了巨大进展,主要是通过使用生物物理和计算技术,这些技术能够对蛋白质中一系列不同扰动的影响进行系统和定量分析。然而,此类分析结果与疾病动物模型中的观察结果之间的相关性受到它们在方法和范围上看似不可调和的差异的限制。不过,最近的几项研究已开始通过结合这两种方法来克服这一限制。这种策略使得在体外广泛而详细的研究得出的基本物理化学原理的背景下,研究蛋白质错误折叠在体内的许多后果成为可能,从疾病发病机制到表观遗传调控。