Structural studies of Togaviruses

披膜病毒的结构研究

• 批准号: 8792826
• 负责人: MICHAEL G ROSSMANN
• 金额: $ 64.23万
• 依托单位: PURDUE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-02-20 至 2016-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8792826
• 关键词: Africa; Alphavirus; Antibodies; Applications Grants; Asia; Capsid Proteins; Cell fusion; Cells; Chikungunya virus; Collaborations; Complex; Cryoelectron Microscopy; Crystallography; Cytoplasm; Dependence; Electron Microscopy; Electrons; Endocytosis; Fab Immunoglobulins; Family; Gene Order; Genome; Glycoproteins; Grant; Health; Homologous Gene; Human; Image; Immunoglobulin Fragments; India; Individual; Infection; Investigation; Life Cycle Stages; Lipids; Maps; Membrane Lipids; Microscopic; Monoclonal Antibodies; Morphology; NIH Vaccine Research Center; Nucleocapsid; Peptide antibodies; Peptides; Play; Process; Recombinants; Resolution; Role; Rubella virus; Sindbis Virus; Southeastern Asia; Staging; Structure; Surface; Techniques; Technology; Togaviridae; Tomogram; Vaccines; Viral; Viral Proteins; Virion; Virus; Virus Inhibitors; Virus-like particle; Work; World Health; X-Ray Crystallography; base; design; electron density; electron tomography; improved; inhibitor/antagonist; insight; mutant; neutralizing antibody; neutralizing monoclonal antibodies; particle; pathogen; polypeptide; receptor; reconstruction; structural biology; tool; virology

DESCRIPTION (provided by applicant: Crystallography was the primary structural tool that first opened up structural investigation of viruses at near-atomic resolution. However, larger viruses with lipid envelopes are too variable in their structures and have too small a proportion of their surface involved in lattice contacts to make stable crystals. Cryo-electron microscopy later emerged as the leading tool for advancing Structural Biology to give the "big picture", with crystallography playing a supporting role in the determination of the crystallizable viral components. Single particle averaging of cryo-electron microscopic images is now approaching almost atomic resolution in favorable cases but, once again, the limits of this technology are becoming apparent in the investigations of progressively more complex pleomorphic assemblies. Cryo-electron tomography has now emerged as an invaluable tool for the determination of the structure of individual viral particles without reliance on averaging between symmetrically equivalent components or on the availability of identical homogeneous particles. However, the resolution of a tomographic reconstruction is insufficient to determine structure in atomic detail. Thus, a part of this grant application is dedicated towards extracting more information from tomograms, especially as applied to the slightly pleomorphic, structurally largely unknown, Rubella virus. Alphaviruses and Rubella virus constitute the Togavirus family because of their similarity in gene order and morphology. Among alphaviruses, Chikungunya virus is a major world health concern because of its recent re-emergence in Asia and Africa. We plan to extend our previous studies of the icosahedral, lipid containing alphaviruses, and tackle the more difficult structural analysis of pleomorphic Rubella virus. Specifically, we are planning to extend the resolution of Chikungunya virus-like particles to near-atomic resolution using cryo-electron microscopy in part as an aid to the design of a vaccine against Chikungunya virus with Gary Nabel at the NIH Vaccine Research Center. We also plan to determine the structure of Rubella virus by analyses of electron tomograms. We plan to use antibodies and peptide inhibitors to block maturation, attachment and fusion with host cells in order to study the structural intermediates encountered in the viral life cycle. We are planning to determine the remaining unknown structures of the Rubella virus components and use both crystallography and electron microscopy to study their interactions with each other and with antibodies.

描述（由申请方提供）：晶体学是首次以近原子分辨率开展病毒结构研究的主要结构工具。然而，具有脂质包膜的较大病毒的结构变化太大，并且参与晶格接触的表面比例太小，无法形成稳定的晶体。冷冻电子显微镜后来成为推进结构生物学的主要工具，以提供“大局”，晶体学在确定可结晶病毒成分方面发挥了支持作用。单粒子平均的低温电子显微镜图像现在接近几乎原子的分辨率在有利的情况下，但再一次，这种技术的局限性越来越明显，在调查越来越复杂的多晶组装。冷冻电子断层扫描现在已经成为一个宝贵的工具，用于确定单个病毒颗粒的结构，而不依赖于对称等效成分之间的平均值或相同的均匀颗粒的可用性。然而，层析重建的分辨率不足以确定原子细节的结构。因此，该资助申请的一部分致力于从断层图像中提取更多信息，特别是应用于略微多形性，结构上基本未知的风疹病毒。 甲病毒和风疹病毒构成披膜病毒家族，因为它们在基因顺序和形态上相似。在甲病毒中，基孔肯雅病毒因最近在亚洲和非洲重新出现而成为世界主要健康问题。我们计划扩展我们以前的研究二十面体，含脂质的甲病毒，并解决更困难的多形性风疹病毒的结构分析。具体来说，我们正计划使用低温电子显微镜将基孔肯雅病毒样颗粒的分辨率扩展到近原子分辨率，部分作为与NIH疫苗研究中心的加里纳贝尔一起设计抗基孔肯雅病毒疫苗的辅助手段。我们还计划通过电子断层扫描分析来确定风疹病毒的结构。 我们计划使用抗体和肽抑制剂来阻断成熟、附着和与宿主细胞融合，以研究病毒生命周期中遇到的结构中间体。我们正计划确定风疹病毒成分的剩余未知结构，并使用晶体学和电子显微镜来研究它们之间以及与抗体之间的相互作用。