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Proteomic and molecular analysis of early events in HSV assembly

HSV 组装早期事件的蛋白质组学和分子分析

基本信息

批准号：
9132475
负责人：
DUNCAN W. WILSON
金额：
$ 5.68万
依托单位：
ALBERT EINSTEIN COLLEGE OF MEDICINE, INC
依托单位国家：
美国
项目类别：
财政年份：
2010
资助国家：
美国
起止时间：
2010-04-01 至 2016-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/9132475
关键词：
Proteomic molecular analysis early events

项目摘要

DESCRIPTION (provided by applicant): All Herpes viruses assemble their DNA-packaged capsids in the infected cell nucleus. These capsids then undergo a process unique in biology: they bud into the inner nuclear membrane and pinch off into the perinuclear space to form a primary enveloped particle. These particles subsequently fuse their envelopes with the outer nuclear membrane and the now cytoplasmic capsids undergo a secondary envelopment in the cytoplasm to form the mature virion. At each envelopment step a complex of proteins termed the tegument is assembled between the capsid and envelope and likely drives the envelopment process. The primary enveloped and mature HSV particles are morphologically quite distinct and are believed to contain quite different arrays of tegument and envelope proteins. However the structure and composition of the perinuclear HSV virus (pnHSV) is poorly defined because to date it has only been possible to examine it by ultrastructural studies. In this application I describe methodology that we have developed to purify pnHSV particles in biochemically useful quantities. We propose to extend our ongoing studies by performing a proteomic analysis of the pnHSV and to test the role of cellular proteins which we have already shown to be present. Furthermore, using the model tegument protein vhs we will dissect the molecular mechanism by which a tegument polypeptide is targeted into the enveloping viral particle.

描述（由申请人提供）：所有疱疹病毒在被感染的细胞核内组装其dna包装的衣壳。然后，这些衣壳经历了生物学中独特的过程：它们发芽进入核膜内部，并挤压到核周空间，形成初级被包膜颗粒。这些颗粒随后将它们的包膜与外核膜融合，现在的细胞质衣壳在细胞质中经历二次包膜，形成成熟的病毒粒子。在包膜的每个步骤中，一种称为被膜的蛋白质复合物在衣壳和包膜之间组装，并可能驱动包膜过程。初生的被包膜和成熟的HSV颗粒在形态上非常不同，并且被认为含有完全不同的被膜和包膜蛋白阵列。然而，核周HSV病毒（pnHSV）的结构和组成尚不明确，因为迄今为止只能通过超微结构研究来检查它。在这个应用程序中，我描述了我们开发的纯化pnHSV颗粒的方法，以生物化学有用的数量。我们建议通过对pnHSV进行蛋白质组学分析来扩展我们正在进行的研究，并测试我们已经证明存在的细胞蛋白的作用。此外，利用模型被膜蛋白vhs，我们将剖析被膜多肽被靶向进入包膜病毒颗粒的分子机制。