Super-resolution studies of the entry mechanisms of influenza viruses

流感病毒侵入机制的超分辨率研究

• 批准号: 8204817
• 负责人: XIAOWEI ZHUANG
• 金额: $ 33.76万
• 依托单位: HARVARD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-09-22 至 2014-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8204817
• 关键词: Actins; Adaptor Signaling Protein; Area; Behavior; Binding; Binding Sites; Biochemical; Biological Assay; Biology; Biomedical Research; Cell Communication; Cell physiology; Cell surface; Cells; Cellular Structures; Cellular biology; Clathrin; Clathrin-Coated Vesicles; Complement; Drug Delivery Systems; Electron Microscopy; Endocytosis; Endosomes; Event; Glycolipids; Glycoproteins; Goals; HIV; Health; Human; Human Influenza A Virus; Human Virus; Image; Imaging Techniques; Imaging technology; Individual; Infection; Influenza; Influenza A Virus, H5N1 Subtype; Influenza A virus; Integration Host Factors; Investigation; Laboratories; Lead; Length; Life; Lipids; Mediating; Microscopy; Molecular; Optics; Parasites; Pathway interactions; Patients; Population; Proteins; RNA Interference; Research; Resolution; Shapes; Sialic Acids; Specificity; Structure; TFAP2A gene; Techniques; Testing; Time; Vesicle; Vesicular stomatitis Indiana virus; Viral; Viral Envelope Proteins; Viral Genome; Virion; Virus; Virus Diseases; Virus Replication; anti-influenza; base; coated pit; epsin 1; flu; fluorescence imaging; genome-wide; imaging modality; improved; influenza epidemic; influenzavirus; insight; meetings; molecular scale; nanoscale; novel; pandemic disease; pandemic influenza; pathogen; polymerization; preference; protein complex; public health relevance; receptor; reconstruction; research study; trafficking; ultra high resolution; virology

DESCRIPTION (provided by applicant): Viral infections pose major threats to human health. As parasites that hijack endogenous cellular functions for replication, viruses are also excellent probes for studying cellular processes. Therefore investigations of viral infection mechanisms may not only lead to new therapies against viral diseases but also to a better understanding of fundamental cell biology and host cell-pathogen interactions. This application focuses on the influenza A virus. Our long-term goal is to dissect the influenza infection pathway and to understand the molecular mechanisms underlying individual steps along the infection pathway. In this project, we will focus on the viral entry step, which is a promising target for drug inhibition and for anti-flu therapies. Given the small sizes of the cellular endocytic structures and the virus, imaging with both ultra-high spatial resolution and molecular specificity is required to visualize the molecular details of viral entry. This requirement is difficult to meet with conventional imaging methods especially for living cells. We have recently developed a super-resolution fluorescence imaging technology, stochastic optical reconstruction microscopy (STORM), which provides near-molecular-scale resolution with high molecular specificity for imaging cellular structures. In this project, we will further improve the resolution of STORM and apply this novel technique to investigate the internalization mechanisms of influenza viruses for the first time. These high-resolution fluorescence imaging studies will be complemented by electron microscopy (EM), biochemical, cell biology, and virology assays. We will tackle the following four specific aims. In Aim 1, we will determine the spatio-temporal organization of the endocytic structures internalizing influenza virus, and compare the results with those obtained for other endocytic cargos, to elucidate the molecular mechanisms underlying virus internalization specifically and clathrin-mediated endocytosis in general. While influenza virus binds to cells through cell-surface sialic acids, various experiments suggest that influenza virus entry may require specific protein receptors in addition to sialic acids. In Aim 2, we will explore the molecular identity of the cellular receptor(s) required for influenza infection and investigate how such receptor(s) may guide viral entry. In Aims 3 and 4, we will determine the internalization mechanisms of two pathologically important influenza virus types. In Aim 3, we will investigate the internalization mechanism of the avian H5N1 influenza virus, which poses a pandemic threat, and compare the results to those on the human virus strains. In Aim 4, we will investigate the entry mechanism of filamentous influenza virus, which represents a prominent form of virus isolated from flu patients. We anticipate that results obtained from these studies will not only elucidate the entry mechanisms of influenza virus, but will also provide new insights into fundamental cellular processes, such as endocytosis, as well as host cell-pathogen interactions. PUBLIC HEALTH RELEVANCE: In this project, we will use advanced imaging techniques with nanometer-scale resolution, together with biochemical, cell biology and virology assays, to investigate the infection mechanisms of influenza viruses, with particular emphasis on viral entry mechanisms. We anticipate that results from these studies will not only help elucidate the infection mechanisms of influenza viruses but will also provide new insights into fundamental cellular processes and into host cell-pathogen interactions. Furthermore, the super-resolution imaging approach developed here will have broad applications in many areas of biomedical research.

描述（由申请人提供）：病毒感染对人类健康构成重大威胁。作为劫持内源性细胞功能进行复制的寄生虫，病毒也是研究细胞过程的极好探针。因此，对病毒感染机制的研究不仅可能导致针对病毒性疾病的新疗法，而且还可以更好地理解基础细胞生物学和宿主细胞-病原体相互作用。该应用程序侧重于甲型流感病毒。我们的长期目标是剖析流感感染途径，并了解感染途径沿着各个步骤的分子机制。在这个项目中，我们将专注于病毒进入步骤，这是一个有前途的药物抑制和抗流感治疗的目标。鉴于细胞内吞结构和病毒的小尺寸，需要超高空间分辨率和分子特异性的成像来可视化病毒进入的分子细节。传统的成像方法难以满足这一要求，尤其是对于活细胞。我们最近开发了一种超分辨率荧光成像技术，随机光学重建显微镜（STORM），它提供了近分子尺度的分辨率与高分子特异性成像细胞结构。在本项目中，我们将进一步提高STORM的分辨率，并首次将这种新技术应用于研究流感病毒的内化机制。这些高分辨率荧光成像研究将由电子显微镜（EM），生物化学，细胞生物学和病毒学分析补充。我们将致力于实现以下四个具体目标。在目的1中，我们将确定流感病毒内化的内吞结构的时空组织，并将结果与其他内吞货物的结果进行比较，以阐明病毒内化的分子机制和网格蛋白介导的内吞作用。虽然流感病毒通过细胞表面唾液酸与细胞结合，但各种实验表明，流感病毒进入可能需要除唾液酸之外的特异性蛋白受体。在目标2中，我们将探索流感感染所需的细胞受体的分子特性，并研究这些受体如何引导病毒进入。在目标3和4中，我们将确定两种病理上重要的流感病毒类型的内化机制。在目标3中，我们将研究H5 N1禽流感病毒的内在化机制，并将其结果与人类病毒株的结果进行比较。在目标4中，我们将研究丝状流感病毒的进入机制，丝状流感病毒代表了从流感患者中分离的病毒的主要形式。我们预计，从这些研究中获得的结果将不仅阐明流感病毒的进入机制，但也将提供新的见解基本的细胞过程，如内吞作用，以及宿主细胞-病原体相互作用。 公共卫生关系：在这个项目中，我们将使用具有纳米级分辨率的先进成像技术，结合生物化学，细胞生物学和病毒学分析，研究流感病毒的感染机制，特别是病毒进入机制。我们预计这些研究的结果不仅有助于阐明流感病毒的感染机制，而且还将为基本细胞过程和宿主细胞-病原体相互作用提供新的见解。此外，这里开发的超分辨率成像方法将在生物医学研究的许多领域中具有广泛的应用。