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Paramyxovirus Membrane Fusion

Paramyxovirus Membrane Fusion
副粘病毒膜融合
批准号:
6473756
负责人:
Trudy G. Morrison
金额:
$19.81万
依托单位国家:
美国
项目类别:
财政年份:
1991
资助国家:
美国
项目状态:
已结题
起止时间:
1991-01-01 至 2006-03-31

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项目成果

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中文摘要
翻译
描述(由申请人提供):我们学习的目的是了解 新城疫病毒副粘病毒膜融合的分子机制 以疾病病毒为原型。与大多数副粘病毒系统一样,膜融合 需要HN和F两种蛋白质。我们的研究集中在F蛋白是如何 介导膜融合和HN蛋白在这一过程中的作用。我们有 最近提出了四个与未解决的问题有直接关系的观察结果 关于副粘病毒融合的问题。首先,我们发现了一个特定的 F蛋白的结构域与HN蛋白的一个结构域相互作用 来自两个蛋白质的序列之间相互作用的直接证据 确定所涉及的F蛋白的特定结构域。第二,使用抗血清 针对F蛋白的HR1和HR2结构域,我们已经证明了构象 依赖于HN蛋白表达的F蛋白和F蛋白的差异 乳沟。第三,使用针对HN短序列的多肽抗血清 蛋白质,我们已经证明了HN蛋白相关的构象差异 到F蛋白的表达和切割。第四,我们提出了一个突变点 F蛋白消除了对HN蛋白的绝对需求 合胞体的形成,这一发现引发了对HN作用的质疑 融合中的蛋白质附着。为了解决这些发现提出的问题 我们提出了四个具体的目标:1)描述特定的 HN蛋白和F蛋白的结构域,2)表征构象变化 在与HN蛋白表达和F蛋白切割相关的F蛋白中,3) HN蛋白与HN蛋白相关的构象变化特征 黏附和F蛋白表达及卵裂。4)探索 在融合开始时的依附。
英文摘要
DESCRIPTION (Provided by applicant): The goal of our studies is to understand the molecular mechanisms of paramyxovirus membrane fusion using Newcastle disease virus as a prototype. As in most paramyxovirus systems, membrane fusion requires both HN and F proteins. Our studies have focused on how F protein mediates membrane fusion and the role of HN protein in that process. We have recently made four observations that have a direct bearing on unresolved questions about paramyxovirus fusion. First, we have found that a specific domain of the F protein interacts with a domains of the HN protein providing direct evidence for an interaction between sequences from the two proteins and identifying specific domains of the F protein involved. Second, using antisera specific for F protein HR1 and HR2 domains, we have demonstrated conformational differences in F protein dependent upon HN protein expression and F protein cleavage. Third, using peptide antisera specific for a short sequence of the HN protein, we have demonstrated conformational differences in HN protein related to F protein expression and cleavage. Fourth, we have made a point mutant in the F protein that eliminates the absolute requirement for HN protein in syncytia formation, a finding that raises questions about the role of HN protein attachment in fusion. To address the questions raised by these findings we propose four specific aims: 1) characterize interactions between specific domains of the HN protein and F protein, 2) characterize conformational changes in the F protein related to HN protein expression and F protein cleavage, 3) characterize conformational changes in the HN protein related to HN protein attachment and F protein expression and cleavage. 4) explore the role of attachment in initiation of fusion.
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