IRIM, CNRS UMR9004, CNRS & University of Montpellier, 34293 Montpellier, France.
Viruses. 2019 Jan 16;11(1):72. doi: 10.3390/v11010072.
The HIV-1 assembly process is a multi-complex mechanism that takes place at the host cell plasma membrane. It requires a spatio-temporal coordination of events to end up with a full mature and infectious virus. The molecular mechanisms of HIV-1 assembly have been extensively studied during the past decades, in order to dissect the respective roles of the structural and non-structural viral proteins of the viral RNA genome and of some host cell factors. Nevertheless, the time course of HIV-1 assembly was observed in living cells only a decade ago. The very recent revolution of optical microscopy, combining high speed and high spatial resolution, in addition to improved fluorescent tags for proteins, now permits study of HIV-1 assembly at the single molecule level within living cells. In this review, after a short description of these new approaches, we will discuss how HIV-1 assembly at the cell plasma membrane has been revisited using advanced super resolution microscopy techniques and how it can bridge the study of viral assembly from the single molecule to the entire host cell.
HIV-1 组装过程是一个发生在宿主细胞质膜上的多复杂机制。它需要事件的时空协调,最终形成完整成熟和有感染力的病毒。在过去的几十年中,为了剖析病毒 RNA 基因组的结构和非结构病毒蛋白以及一些宿主细胞因子的各自作用,人们对 HIV-1 组装的分子机制进行了广泛的研究。然而,仅在十年前,人们才在活细胞中观察到 HIV-1 的组装过程。最近,光学显微镜技术的革命性进展,结合了高速和高空间分辨率,以及对蛋白质的改进荧光标记,现在使得在活细胞内的单分子水平上研究 HIV-1 组装成为可能。在本文综述中,在简要描述这些新方法之后,我们将讨论如何使用先进的超分辨率显微镜技术重新研究细胞质膜上的 HIV-1 组装,以及它如何将病毒组装的研究从单分子水平扩展到整个宿主细胞。