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实时成像个体病毒粒子触发的皮层肌动蛋白动力学,用于研究人类免疫缺陷病毒进入静止 CD4 T 细胞的过程。

Real-time imaging of individual virion-triggered cortical actin dynamics for human immunodeficiency virus entry into resting CD4 T cells.

机构信息

State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, People's Republic of China.

National Center for Biodefense and Infectious Diseases, Department of Molecular and Microbiology, George Mason University, Manassas, Virginia 22030, USA.

出版信息

Nanoscale. 2020 Jan 7;12(1):115-129. doi: 10.1039/c9nr07359k. Epub 2019 Nov 27.

Abstract

Real-time imaging of single virus particles allows the visualization of subtle dynamic events of virus-host interaction. During the human immunodeficiency virus (HIV) infection of resting CD4 T lymphocytes, overcoming cortical actin restriction is an essential step, but the dynamic process and mechanism remain to be characterized. Herein, by using quantum dot (QD) encapsulated fluorescent viral particles and single-virus tracking, we explored detailed scenarios of HIV dynamic entry and crossing the cortical actin barrier. The fine-scale temporal and spatial processes of single HIV virion interaction with the cortical actin were studied in depth during virus entry via plasma membrane fusion. Individual HIV virions modulate the subtle rearrangement of the cortical actin barrier to open a door to facilitate viral entry. The actin-binding protein, α-actinin, was found to be critical for actin dynamics during HIV entry. An α-actinin-derived peptide, actin-binding site 1 peptide (ABS1p), was developed to block HIV infection. Our findings reveal an α-actinin-mediated dynamic cortical actin rearrangement for HIV entry, and identify an antiviral target as well as a corresponding peptide inhibitor based on HIV interaction with the actin cytoskeleton.

摘要

实时成像单个病毒颗粒可使病毒-宿主相互作用的微妙动态事件可视化。在人类免疫缺陷病毒(HIV)感染静止的 CD4 T 淋巴细胞期间,克服皮质肌动蛋白的限制是一个重要步骤,但动态过程和机制仍有待描述。在此,通过使用量子点(QD)封装的荧光病毒颗粒和单病毒跟踪,我们探索了 HIV 动态进入和穿过皮质肌动蛋白障碍的详细情况。通过质膜融合,深入研究了单个 HIV 病毒颗粒与皮质肌动蛋白相互作用的精细时空过程,以了解病毒进入过程。单个 HIV 病毒颗粒调节皮质肌动蛋白障碍的细微重排,为病毒进入开辟通道。发现肌动蛋白结合蛋白 α-辅肌动蛋白对于 HIV 进入期间的肌动蛋白动力学至关重要。开发了一种源自 α-辅肌动蛋白的肽,即肌动蛋白结合位点 1 肽(ABS1p),以阻止 HIV 感染。我们的研究结果揭示了 HIV 进入过程中肌动蛋白结合蛋白介导的动态皮质肌动蛋白重排,并确定了抗病毒靶标以及基于 HIV 与肌动蛋白细胞骨架相互作用的相应肽抑制剂。

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