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Investigation of SV5 Budding Mechanisms

SV5 出芽机制的研究

基本信息

批准号：
8046367
负责人：
ANTHONY P SCHMITT
金额：
$ 31.37万
依托单位：
PENNSYLVANIA STATE UNIVERSITY, THE
依托单位国家：
美国
项目类别：
财政年份：
2007
资助国家：
美国
起止时间：
2007-04-01 至 2013-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8046367
关键词：
ATP phosphohydrolase Affect Affinity Chromatography Animals Antiviral Agents Binding Cellular Membrane Development Disease Dominant-Negative Mutation Drug Delivery Systems E protein Electron Microscopy Excision Filovirus Foundations Future HIV-1 Human Individual Integration Host Factors Investigation Libraries Lysine Maps Measles Mediating Membrane Mumps NP protein Paramyxovirus Pathway interactions Process Production Proteasome Inhibitor Protein Binding Protein Binding Domain Proteins Public Health Recruitment Activity Research Personnel Retroviridae Rhabdoviridae Role Scheme Site Testing Ubiquitin Ubiquitination Viral Viral Matrix Proteins Virus Virus Assembly Virus-like particle Yeasts defined contribution multicatalytic endopeptidase complex multiple myeloma M Protein mutant parainfluenza virus particle prevent programs protein function recombinant virus research study simian virus 5 nucleocapsid protein yeast two hybrid system

项目摘要

DESCRIPTION (provided by applicant): Enveloped viruses are formed by a budding process that occurs following the assembly of viral components at cellular membranes. The late steps leading up to membrane fission and particle release appear to be accomplished in many cases through manipulation of host machinery that is recruited to virus assembly sites. As paramyxoviruses lack the same late domain sequences used by many other enveloped viruses, such as retroviruses, for host factor recruitment, the steps leading up to the release of paramyxovirus particles are poorly understood. Recently, we identified an alternative sequence, FPIV, within the matrix (M) protein of the paramyxovirus parainfluenza virus 5 (SV5) that can functionally substitute for the PTAP late domain of human immunodeficiency virus type 1 (HIV-1) for budding. Here, we propose experiments to further investigate mechanisms by which paramyxoviruses manipulate host machinery to facilitate virus budding. Our first aim is to investigate the role of the ubiquitin-proteasome pathway in SV5 budding by testing the possibility that SV5 M protein is a direct target for the attachment of ubiquitin molecules. We will attempt to prevent this ubiquitination from occurring through removal of lysine residues near the FPIV sequence of M protein. Our second aim is to define the subset of individual Class E proteins that is important for SV5 budding and that is recruited to SV5 assembly sites. Our third aim is to identify host proteins that bind to SV5 M protein, test the importance of M-interacting proteins for SV5 budding, and assess whether binding occurs in a way that is dependent on the FPIV sequence. Our fourth aim is to investigate the unique role of SV5 NP protein in the budding of virus-like particles. Relevance to public health: Paramyxoviruses are responsible for a wide range of diseases that affect both humans and animals, including measles and mumps. A better understanding of paramyxovirus budding will provide a foundation for future efforts towards the development of antiviral drugs that target this step of the virus lifecycle.

描述(申请人提供)：包膜病毒是在病毒成分在细胞膜上组装后的萌发过程中形成的。在许多情况下，导致膜分裂和颗粒释放的后期步骤似乎是通过操纵宿主机器完成的，这些宿主机器被招募到病毒组装部位。由于副粘病毒缺乏许多其他包膜病毒(如逆转录病毒)用于宿主因子招募的晚期结构域序列，导致副粘病毒颗粒释放的步骤尚不清楚。最近，我们在副粘病毒副流感病毒5(SV5)的基质(M)蛋白中发现了一个替代序列，FPIV，它可以在功能上取代人类免疫缺陷病毒1型(HIV-1)的PTAP晚期结构域。在这里，我们建议进行实验，以进一步研究副粘病毒操纵宿主机制以促进病毒萌发的机制。我们的第一个目标是通过测试SV5 M蛋白是泛素分子直接结合的目标的可能性来研究泛素-蛋白酶体途径在SV5发芽中的作用。我们将试图通过去除M蛋白的FPIV序列附近的赖氨酸残基来防止这种泛素化的发生。我们的第二个目标是确定单个E类蛋白的子集，它对SV5的萌发很重要，并被招募到SV5组装位置。我们的第三个目标是鉴定与SV5 M蛋白结合的宿主蛋白，测试M相互作用蛋白对SV5发芽的重要性，并评估结合是否以依赖于FPIV序列的方式发生。我们的第四个目标是研究SV5 NP蛋白在病毒样颗粒萌发中的独特作用。与公共卫生相关：副粘病毒可引起多种影响人类和动物的疾病，包括麻疹和流行性腮腺炎。对副粘病毒萌发的更好了解将为今后针对病毒生命周期这一阶段开发抗病毒药物的努力提供基础。