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热休克蛋白90:HIV-1的伴侣蛋白。

Hsp90: a chaperone for HIV-1.

作者信息

Low Jun Siong, Fassati Ariberto

机构信息

The Wohl Virion Centre, MRC Centre for Medical Molecular Virology,Division of Infection & Immunity, UCL, Cruciform Building, 90 Gower Street, London WC1E 6BT,UK.

出版信息

Parasitology. 2014 Aug;141(9):1192-202. doi: 10.1017/S0031182014000298.

Abstract

HIV-1 replication has been intensively investigated over the past 30 years. Hsp90 is one of the most abundant proteins in human cells, important in the formation and function of several protein complexes that maintain cell homeostasis. Remarkably, the impact of Hsp90 on HIV-1 infection has started to be appreciated only recently. Hsp90 has been shown to (a) promote HIV-1 gene expression in acutely infected cells, (b) localize at the viral promoter DNA, (c) mediate enhanced replication in conditions of hyperthermia and (d) activate the P-TEFb complex, which is essential for efficient HIV-1 transcription. Hsp90 has been implicated in buffering deleterious mutations of the viral core and in the regulation of innate and acquired immune responses to HIV-1 infection. Therefore, Hsp90 is an important host factor promoting several steps of the HIV-1 life cycle. Several small Hsp90 inhibitors are in Phase II clinical trials for human cancers and might potentially be used to inhibit HIV-1 infection at multiple levels.

摘要

在过去30年里,人们对HIV-1复制进行了深入研究。热休克蛋白90(Hsp90)是人类细胞中含量最丰富的蛋白质之一,对维持细胞稳态的几种蛋白质复合物的形成和功能至关重要。值得注意的是,直到最近Hsp90对HIV-1感染的影响才开始受到重视。研究表明,Hsp90能够:(a)促进急性感染细胞中HIV-1基因的表达;(b)定位于病毒启动子DNA;(c)在高温条件下介导病毒复制增强;(d)激活P-TEFb复合物,这对HIV-1的高效转录至关重要。Hsp90还与缓冲病毒核心的有害突变以及调节对HIV-1感染的先天性和获得性免疫反应有关。因此,Hsp90是促进HIV-1生命周期多个步骤的重要宿主因子。几种小型Hsp90抑制剂正处于人类癌症的II期临床试验阶段,可能会被用于在多个层面抑制HIV-1感染。

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