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成孔蛋白毒素:从结构到功能

Pore-forming protein toxins: from structure to function.

作者信息

Parker Michael W, Feil Susanne C

机构信息

Biota Structural Biology Laboratory, St. Vincent's Institute of Medical Research, 9 Princes Street, Fitzroy, Victoria 3065, Australia.

出版信息

Prog Biophys Mol Biol. 2005 May;88(1):91-142. doi: 10.1016/j.pbiomolbio.2004.01.009.

Abstract

Pore-forming protein toxins (PFTs) are one of Nature's most potent biological weapons. An essential feature of their toxicity is the remarkable property that PFTs can exist either in a stable water-soluble state or as an integral membrane pore. In order to convert from the water-soluble to the membrane state, the toxin must undergo large conformational changes. There are now more than a dozen PFTs for which crystal structures have been determined and the nature of the conformational changes they must undergo is beginning to be understood. Although they differ markedly in their primary, secondary, tertiary and quaternary structures, nearly all can be classified into one of two families based on the types of pores they are thought to form: alpha-PFTs or beta-PFTs. Recent work suggests a number of common features in the mechanism of membrane insertion may exist for each class.

摘要

成孔蛋白毒素(PFTs)是自然界中最强大的生物武器之一。其毒性的一个基本特征是PFTs具有显著特性,即它们既可以以稳定的水溶性状态存在,也可以作为完整的膜孔存在。为了从水溶性状态转变为膜状态,毒素必须经历巨大的构象变化。目前已有十多种PFTs的晶体结构被确定,并且它们必须经历的构象变化的性质也开始被理解。尽管它们在一级、二级、三级和四级结构上有显著差异,但几乎所有的PFTs都可以根据它们被认为形成的孔的类型分为两个家族之一:α-PFTs或β-PFTs。最近的研究表明,每一类在膜插入机制中可能存在一些共同特征。

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