Laboratory of Retrovirology, The Rockefeller University, New York, NY 10016, USA.
J Mol Biol. 2011 Jul 22;410(4):501-11. doi: 10.1016/j.jmb.2011.04.062.
The assembly of an HIV-1 particle is a complex, multistep process involving several viral and cellular proteins, RNAs and lipids. While many macroscopic and fixed-cell microscopic techniques have provided important insights into the structure of HIV-1 particles and the mechanisms by which they assemble, analysis of individual particles and their assembly in living cells offers the potential of surmounting many of the limitations inherent in other approaches. In this review, we discuss how the recent application of live-cell microscopic imaging techniques has increased our understanding of the process of HIV-1 particle assembly. In particular, we focus on recent studies that have employed total internal reflection fluorescence microscopy and other single-virion imaging techniques in live cells. These approaches have illuminated the dynamics of Gag protein assembly, viral RNA packaging and ESCRT (endosomal sorting complex required for transport) protein recruitment at the level of individual viral particles. Overall, the particular advantages of individual particle imaging in living cells have yielded findings that would have been difficult or impossible to obtain using macroscopic or fixed-cell microscopic techniques.
HIV-1 颗粒的组装是一个复杂的、多步骤的过程,涉及几种病毒和细胞蛋白、RNA 和脂质。虽然许多宏观和固定细胞显微镜技术为了解 HIV-1 颗粒的结构以及它们组装的机制提供了重要的见解,但对单个颗粒及其在活细胞中组装的分析提供了克服其他方法固有限制的潜力。在这篇综述中,我们讨论了最近应用活细胞显微镜成像技术如何提高我们对 HIV-1 颗粒组装过程的理解。特别是,我们关注了最近在活细胞中使用全内反射荧光显微镜和其他单病毒成像技术的研究。这些方法阐明了在单个病毒颗粒水平上 Gag 蛋白组装、病毒 RNA 包装和 ESCRT(内体分选复合物必需的运输)蛋白募集的动力学。总的来说,活细胞中单颗粒成像的特殊优势产生了一些发现,如果使用宏观或固定细胞显微镜技术,这些发现将很难或不可能获得。