Institut Pasteur, Virus and Immunity Unit, CNRS-UMR3569, Paris, France.
Paris Diderot University, Sorbonne Paris Cité, Paris, France.
J Virol. 2020 Feb 28;94(6). doi: 10.1128/JVI.01783-19.
The HIV-1 Env protein is exposed at the surface of virions and infected cells. Env fluctuates between different closed and open structural states and these conformations influence both viral infectivity and sensitivity to antibody binding and neutralization. We established a flow virometry assay to visualize Env proteins at the surface of human immunodeficiency virus type 1 (HIV-1) virions. The assay is performed on ultracentrifuged fluorescent viral particles that are stained with a panel of broadly neutralizing antibodies (bNAbs) and nonneutralizing antibodies (nnAbs) that probe different epitopes of Env. We used this assay to compare Env at the surface of producer cells and viral particles and to analyze the effect of Nef, CD4, and SERINC5 on Env accessibility to antibodies. We studied the laboratory-adapted strain NL4-3 and two transmitted/founder viruses, THRO and CH058. We confirm that antibody accessibility varies between viral strains and show that Nef, CD4, and SERINC5 additively impact Env conformations. We further demonstrate that the Env accessibility profile on virions is globally similar to that observed on HIV-1-infected cells, with some noticeable differences. For instance, nnAbs bind to virions more efficiently than to producer cells, likely reflecting changes in Env conformational states on mature viral particles. This test complements other techniques and provides a convenient and simple tool for quantifying and probing the structure of Env at the virion surface and to analyze the impact of viral and cellular proteins on these parameters. HIV-1 Env conformation is one of the key parameters determining viral infectivity. The flow virometry-based assay developed in this study allows for the characterization of proteins incorporated in HIV-1 particles. We studied the conformation of HIV-1 Env and the impact that the viral protein Nef and the cellular proteins CD4 and SERINC5 have on Env accessibility to antibodies. Our assay permitted us to highlight some noticeable differences in the conformation of Env between producer cells and viral particles. It contributes to a better understanding of the actual composition of HIV-1 particles.
HIV-1 包膜蛋白(Env 蛋白)暴露在病毒粒子和感染细胞的表面。Env 蛋白在不同的封闭和开放结构状态之间波动,这些构象影响病毒的感染力以及对抗体结合和中和的敏感性。我们建立了一种流式病毒测量法来可视化人类免疫缺陷病毒 1 型(HIV-1)病毒粒子表面的 Env 蛋白。该测定法在超离心荧光病毒粒子上进行,这些粒子用一组广泛中和抗体(bNAbs)和非中和抗体(nnAbs)进行染色,这些抗体探测 Env 的不同表位。我们使用该测定法比较了产生细胞和病毒粒子表面的 Env,并分析了 Nef、CD4 和 SERINC5 对 Env 与抗体可及性的影响。我们研究了实验室适应株 NL4-3 和两种传播/起始病毒,THRO 和 CH058。我们证实,抗体可及性在不同病毒株之间存在差异,并表明 Nef、CD4 和 SERINC5 可累加影响 Env 构象。我们进一步表明,病毒粒子上的 Env 可及性谱与观察到的 HIV-1 感染细胞上的谱总体上相似,但存在一些明显差异。例如,nnAbs 比在产生细胞上更有效地结合病毒粒子,这可能反映了成熟病毒粒子上 Env 构象状态的变化。该测试补充了其他技术,并提供了一种方便而简单的工具,用于定量和探测病毒粒子表面 Env 的结构,并分析病毒和细胞蛋白对这些参数的影响。HIV-1 Env 构象是决定病毒感染力的关键参数之一。本研究中开发的基于流式病毒测量的测定法允许对 HIV-1 颗粒中包含的蛋白质进行表征。我们研究了 HIV-1 Env 的构象以及病毒蛋白 Nef 和细胞蛋白 CD4 和 SERINC5 对 Env 与抗体可及性的影响。我们的测定法使我们能够突出产生细胞和病毒粒子之间 Env 构象的一些明显差异。它有助于更好地理解 HIV-1 颗粒的实际组成。