Single virions to study assembly of HIV-1

单一病毒体研究 HIV-1 的组装

• 批准号: 9270040
• 负责人: SANFORD M SIMON
• 金额: $ 33.48万
• 依托单位: ROCKEFELLER UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-05-05 至 2020-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9270040
• 关键词: ABCE1 gene; ATP phosphohydrolase; Affect; Anisotropy; Appearance; Biochemical; Biogenesis; Biological Assay; CRISPR/Cas technology; Cell Line; Cell membrane; Cells; Color; DegP protease; Dimensions; Dimerization; Endocytosis; Endosomes; Event; Fluorescence Microscopy; Fluorescence Resonance Energy Transfer; Genome; Goals; HIV; HIV-1; Image; Individual; Infection; Kinetics; Label; Ligase; Link; Location; Membrane; Microscopy; Monitor; Mothers; Movement; Neck; Nucleotides; Optics; Organelles; Peptide Hydrolases; Play; Point Mutation; Population; Process; Production; Proteins; Recruitment Activity; Resolution; Retroviridae; Role; Site; Structure; Techniques; Technology; Testing; Tissues; Viral; Virion; Virus; Virus Assembly; base; dimer; experimental study; extracellular; fluorophore; gag Gene Products; helicase; monomer; particle; public health relevance; sensor; spatial relationship

 DESCRIPTION (provided by applicant): The productive site of HIV-1 assembly is the plasma membrane, both in cultured cell lines and primary cells. This conclusion is based both on the observation that newly synthesized Gag first appears at the plasma membrane, and is only detected later in endosomes, and the demonstration that inhibiting endocytosis blocks the appearance of virions in the internal organelles without affecting the yield of extracellular particles This assembly of HIV-1 at the plasma membrane make the assembly accessible to imaging using total internal reflection fluorescence microscopy (TIR-FM) a technique on which a large fraction of the experiments in this proposal are based. This technique has been used to visualize individual virions of HIV-1 as they assemble as well as the movement and packaging of individual molecules or dimers of HIV-1 genome. The technique has been used to demonstrate that the virions accumulate at the plasma membrane over a period of 6-20 minutes. The genome is recruited to the plasma membrane immediately before recruitment of Gag. In contrast, ESCRTs are recruited for only tens of seconds and tens of molecules transiently at the very end of the recruitment of Gag. The AAA-ATPase, Vps4, is recruited just seconds later. Super-resolution optical microscopy has added the information that ESCRT recruitment is to the neck that links the nascent virion to the mother cell. The long-term goal of this project is to identify, characterize and ultimately understand the steps in the biogenesis of HIV-1 and related retroviruses. We want to understand the dynamics of viral components as they interact with each other and with host components. Imaging based approaches allow the examination of both the dynamics and localization of molecules during which may be inaccessible through biochemical techniques. The main foci will be on the dynamics and localization of the viral protein Gag, the dynamics and localization of host molecules and then the relative dynamics and localization of the viral and host molecules.

 描述（由申请方提供）：HIV-1组装的生产位点是质膜，在培养的细胞系和原代细胞中均是如此。这一结论是基于新合成的Gag首先出现在质膜上，并且随后仅在内体中检测到，并且证明了抑制内吞作用阻断了病毒体在内部细胞器中的出现而不影响细胞外颗粒的产量。HIV-1在质膜上的这种组装使得该组装可以使用全内反射荧光显微镜成像（TIR-FM），该提议中的大部分实验基于该技术。该技术已被用于可视化HIV-1的单个病毒体，因为它们组装以及单个分子或HIV-1基因组二聚体的运动和包装。该技术已被用于证明病毒体在6-20分钟的时间内在质膜上积累。基因组在Gag募集之前立即被募集到质膜。相比之下，ESCRT仅募集数十秒，并且在Gag募集的最后瞬间募集数十个分子。AAA-ATPase，Vps 4，在几秒钟后被招募。超分辨率光学显微镜增加了ESCRT募集是连接新生病毒体与母细胞的颈部的信息。该项目的长期目标是识别、表征并最终了解HIV-1和相关逆转录病毒的生物合成步骤。我们希望了解病毒成分相互作用以及与宿主成分相互作用的动力学。基于成像的方法允许检查分子的动力学和定位，在此期间可能无法通过生物化学技术进行。主要焦点将是病毒蛋白Gag的动力学和定位，宿主分子的动力学和定位，然后是病毒和宿主分子的相对动力学和定位。