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EAP45与出芽的HIV-1的关联:动力学和结构域要求。

EAP45 association with budding HIV-1: Kinetics and domain requirements.

作者信息

Meng Bo, Vallejo Ramirez Pedro P, Scherer Katharina M, Bruggeman Ezra, Kenyon Julia C, Kaminski Clemens F, Lever Andrew M

机构信息

Department of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.

Laser Analytics Group, Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge, UK.

出版信息

Traffic. 2021 Dec;22(12):439-453. doi: 10.1111/tra.12820. Epub 2021 Oct 3.

Abstract

A number of viruses including HIV use the ESCRT system to bud from the infected cell. We have previously confirmed biochemically that ESCRT-II is involved in this process in HIV-1 and have defined the molecular domains that are important for this. Here, using SNAP-tag fluorescent labelling and both fixed and live cell imaging we show that the ESCRT-II component EAP45 colocalises with the HIV protein Gag at the plasma membrane in a temporal and quantitative manner, similar to that previously shown for ALIX and Gag. We show evidence that a proportion of EAP45 may be packaged within virions, and we confirm the importance of the N terminus of EAP45 and specifically the H0 domain in this process. By contrast, the Glue domain of EAP45 is more critical for recruitment during cytokinesis, emphasising that viruses have ways of recruiting cellular components that may be distinct from those used by some cellular processes. This raises the prospect of selective interference with the pathway to inhibit viral function while leaving cellular functions relatively unperturbed.

摘要

包括人类免疫缺陷病毒(HIV)在内的多种病毒利用内体分选转运复合体(ESCRT)系统从被感染细胞中出芽。我们之前已通过生化方法证实ESCRT-II参与了HIV-1的这一过程,并确定了对此过程至关重要的分子结构域。在此,我们使用SNAP标签荧光标记以及固定细胞和活细胞成像技术,表明ESCRT-II组分EAP45与HIV蛋白Gag在质膜上以时间和定量方式共定位,这与之前观察到的ALIX和Gag的情况相似。我们有证据表明一部分EAP45可能被包装在病毒粒子内,并且我们证实了EAP45的N端,特别是H0结构域在此过程中的重要性。相比之下,EAP45的Glue结构域在胞质分裂期间的募集过程中更为关键,这强调了病毒具有招募细胞组分的方式,这些方式可能与某些细胞过程所使用的方式不同。这为选择性干扰该途径以抑制病毒功能同时使细胞功能相对不受干扰带来了前景。

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