HMPV Fusion protein-host cell interactions

HMPV 融合蛋白-宿主细胞相互作用

• 批准号: 7293994
• 负责人: Rebecca E. Dutch
• 金额: $ 18.31万
• 依托单位: UNIVERSITY OF KENTUCKY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-08-15 至 2009-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7293994
• 关键词: Acute; Address; Age; Animal Model; Binding; Biological Assay; Carbohydrates; Cell Communication; Cell Line; Cell Surface Proteins; Cell fusion; Cell membrane; Cell surface; Cells; Cellular Structures; Chemicals; Child; Chimeric Proteins; Cultured Cells; Enzymes; Family; Future; GTP-Binding Proteins; Genes; Glycoproteins; Glycosaminoglycans; Goals; Hamsters; Human; Human Metapneumovirus; Human respiratory syncytial virus; Individual; Infant; Infection; Infectious Agent; Lead; Location; Lung diseases; Mediating; Membrane Fusion; Metapneumovirus; Modification; Paramyxovirus; Paramyxovirus Fusion Protein; Process; Production; Proteins; Proteoglycan; Proteolytic Processing; Reagent; Recombinants; Reporter Genes; Reporting; Research; Respiratory Tract Diseases; Respiratory syncytial virus; Sampling; Sequence Analysis; Staging; Symptoms; Trypsin; Viral; Viral Proteins; Virus; attachment protein G; cell type; crosslink; experience; inhibitor/antagonist; nonhuman primate; pathogen; protein function; receptor; treatment effect

DESCRIPTION (provided by applicant): Human metapneumovirus (HMPV) is a recently identified paramyxovirus associated with severe respiratory disease, particularly in infants, with symptoms that closely resemble those seen with respiratory syncytial virus. We have established efficient assays for the study of membrane fusion promoted by the HMPV fusion (F) glycoprotein. Interestingly, HMPV F protein-mediated cell-cell fusion only occurs when transfected cells are both treated with trypsin (to proteolytically process the HMPV F protein) and exposed to low pH. As previously studied paramyxovirus F proteins promote fusion at neutral pH at the plasma membrane, the triggering of HMPV F protein fusion activity by low pH suggests that this protein functions in a manner unique among the paramyxoviruses. Our results also demonstrate that HMPV F is competent to promote fusion in the absence of the attachment (G) protein, consistent with reports that recombinant HMPV viruses lacking the HMPV G protein replicate efficiently both in cell culture and in hamster and non-human primate animal model. Our long-term goal is to understand the attachment and entry of paramyxoviruses. Our specific hypothesis is that HMPV F interacts with one or more defined cellular receptors, and that this interaction is necessary to prime the F protein for low-pH induced promotion of membrane fusion. To address this hypothesis we will pursue three research aims. First, we will utilize our recently developed, efficient reporter gene assay to systematically define the target cell components required for HMPV F protein-promoted membrane fusion. Second, we will analyze the effect of treatments to the HMPV F protein on promotion of membrane fusion, including effects of prior low pH treatment, proteolytic processing of the F protein or addition of soluble glycosaminoglycans. Finally, we will utilize a soluble form of the HMPV F protein to analyze binding and identify the specific cellular receptor(s) for HMPV F. Accomplishing these goals will provide crucial information on the cellular components that interact with the HMPV F protein, and may well lead to identification of the first receptor for a paramyxovirus fusion protein. In addition, these studies will further clarify the mechanism by which the HMPV F protein promotes critical early steps in infection, and set the stage for future analysis of inhibitors of this important viral protein. Human metapneumovirus (HMPV) is a recently identified human pathogen responsible for significant levels of severe respiratory disease, particularly in infants. This research will address significant questions concerning the cellular factors which interact with the HMPV fusion protein to facilitate attachment of the virus and entry into cells.

描述(申请人提供)：人类偏肺病毒(HMPV)是一种新近发现的与严重呼吸道疾病有关的副粘病毒，尤其是在婴儿中，其症状与呼吸道合胞病毒非常相似。我们建立了研究HMPV融合(F)糖蛋白促进膜融合的有效方法。有趣的是，HMPV F蛋白介导的细胞-细胞融合只有在转基因细胞同时被胰酶处理(以蛋白水解性处理HMPV F蛋白)和暴露在低pH下时才发生。正如先前研究的那样，副粘病毒F蛋白在质膜中性pH下促进融合，低pH触发HMPV F蛋白融合活性表明该蛋白具有副粘病毒所特有的功能。我们的结果还表明，HMPV F在没有附着(G)蛋白的情况下能够促进融合，这与报道的缺乏HMPV G蛋白的重组HMPV病毒在细胞培养以及在仓鼠和非人类灵长类动物模型中都有效复制是一致的。我们的长期目标是了解副粘病毒的附着和进入。我们的特定假设是HMPV F与一个或多个确定的细胞受体相互作用，这种相互作用是启动F蛋白在低pH诱导下促进膜融合所必需的。为了解决这一假设，我们将追求三个研究目标。首先，我们将利用我们最近开发的高效报告基因分析来系统地确定HMPV F蛋白促进膜融合所需的靶细胞成分。其次，我们将分析对HMPV F蛋白的处理对膜融合的促进作用，包括预先的低pH处理、F蛋白的蛋白水解性处理或添加可溶性糖胺多聚糖。最后，我们将利用HMPV F蛋白的一种可溶性形式来分析与HMPV F的结合并鉴定HMPV F的特异性细胞受体(S)。完成这些目标将提供关于与HMPV F蛋白相互作用的细胞成分的关键信息，并很可能导致鉴定副粘病毒融合蛋白的第一个受体。此外，这些研究将进一步阐明HMPV F蛋白促进感染早期关键步骤的机制，并为未来分析这一重要病毒蛋白的抑制剂奠定基础。人类偏肺病毒(HMPV)是最近发现的一种人类病原体，可导致严重的呼吸道疾病，特别是在婴儿中。这项研究将解决与HMPV融合蛋白相互作用以促进病毒附着和进入细胞的细胞因素的重要问题。