EAP45与出芽HIV-1的关联:动力学和结构域要求。

IF 3.6 3区 生物学 Q3 CELL BIOLOGY
Traffic Pub Date : 2021-12-01 Epub Date: 2021-10-03 DOI:10.1111/tra.12820
Bo Meng, Pedro P Vallejo Ramirez, Katharina M Scherer, Ezra Bruggeman, Julia C Kenyon, Clemens F Kaminski, Andrew M Lever
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引用次数: 1

摘要

包括HIV在内的许多病毒使用ESCRT系统从受感染的细胞中发芽。我们之前已经从生物化学角度证实了ESCRT-II参与了HIV-1的这一过程,并确定了对此重要的分子结构域。在这里,使用snap标签荧光标记和固定细胞和活细胞成像,我们显示ESCRT-II组分EAP45与HIV蛋白Gag在质膜上以时间和定量的方式共定位,类似于先前对ALIX和Gag的显示。我们证明了一部分EAP45可能被包装在病毒粒子内,我们证实了EAP45的N端,特别是H0结构域在这一过程中的重要性。相比之下,EAP45的Glue结构域在细胞质分裂过程中对募集更为关键,这强调了病毒募集细胞成分的方式可能与某些细胞过程中使用的方式不同。这提出了选择性干扰途径抑制病毒功能的前景,同时使细胞功能相对不受干扰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EAP45 association with budding HIV-1: Kinetics and domain requirements.

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.

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来源期刊
Traffic
Traffic 生物-细胞生物学
CiteScore
8.10
自引率
2.20%
发文量
50
审稿时长
2 months
期刊介绍: Traffic encourages and facilitates the publication of papers in any field relating to intracellular transport in health and disease. Traffic papers span disciplines such as developmental biology, neuroscience, innate and adaptive immunity, epithelial cell biology, intracellular pathogens and host-pathogen interactions, among others using any eukaryotic model system. Areas of particular interest include protein, nucleic acid and lipid traffic, molecular motors, intracellular pathogens, intracellular proteolysis, nuclear import and export, cytokinesis and the cell cycle, the interface between signaling and trafficking or localization, protein translocation, the cell biology of adaptive an innate immunity, organelle biogenesis, metabolism, cell polarity and organization, and organelle movement. All aspects of the structural, molecular biology, biochemistry, genetics, morphology, intracellular signaling and relationship to hereditary or infectious diseases will be covered. Manuscripts must provide a clear conceptual or mechanistic advance. The editors will reject papers that require major changes, including addition of significant experimental data or other significant revision. Traffic will consider manuscripts of any length, but encourages authors to limit their papers to 16 typeset pages or less.
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