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HIV-1 Env 三聚体在与活 T 细胞结合的天然病毒上的结构动力学。

Structure dynamics of HIV-1 Env trimers on native virions engaged with living T cells.

机构信息

Department of Infectious Diseases, King's College London, Faculty of Life Sciences & Medicine, London, United Kingdom.

Randall Division of Cell and Molecular Biophysics, King's College London, London, United Kingdom.

出版信息

Commun Biol. 2021 Oct 27;4(1):1228. doi: 10.1038/s42003-021-02658-1.

Abstract

The HIV-1 envelope glycoprotein (Env) mediates viral entry into the host cell. Although the highly dynamic nature of Env intramolecular conformations has been shown with single molecule spectroscopy in vitro, the bona fide Env intra- and intermolecular mechanics when engaged with live T cells remains unknown. We used two photon fast fluorescence lifetime imaging detection of single-molecule Förster Resonance Energy Transfer occurring between fluorescent labels on HIV-1 Env on native virions. Our observations reveal Env dynamics at two levels: transitions between different intramolecular conformations and intermolecular interactions between Env within the viral membrane. Furthermore, we show that three broad neutralizing anti-Env antibodies directed to different epitopes restrict Env intramolecular dynamics and interactions between adjacent Env molecules when engaged with living T cells. Importantly, our results show that Env-Env interactions depend on efficient virus maturation, and that is disrupted upon binding of Env to CD4 or by neutralizing antibodies. Thus, this study illuminates how different intramolecular conformations and distribution of Env molecules mediate HIV-1 Env-T cell interactions in real time and therefore might control immune evasion.

摘要

HIV-1 包膜糖蛋白(Env)介导病毒进入宿主细胞。尽管已经通过体外单分子光谱技术证明了 Env 分子内构象的高度动态性质,但与活 T 细胞结合时,真正的 Env 分子内和分子间力学仍不清楚。我们使用双光子快速荧光寿命成像检测技术,检测 HIV-1 Env 上荧光标记物之间发生的单分子Förster 共振能量转移。我们的观察结果揭示了 Env 在两个层面上的动力学:不同分子内构象之间的转变,以及病毒膜内 Env 之间的分子间相互作用。此外,我们还表明,三种针对不同表位的广谱中和抗 Env 抗体在与活 T 细胞结合时,限制了 Env 分子内动力学和相邻 Env 分子之间的相互作用。重要的是,我们的结果表明,Env-Env 相互作用依赖于有效的病毒成熟,而当 Env 与 CD4 结合或被中和抗体结合时,这种相互作用会被破坏。因此,这项研究阐明了不同的分子内构象和 Env 分子的分布如何实时介导 HIV-1 Env-T 细胞相互作用,从而可能控制免疫逃逸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cb0/8551276/fd711b5ed83c/42003_2021_2658_Fig1_HTML.jpg

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