Host factors in the alphavirus replication complex
甲病毒复制复合物中的宿主因子
基本信息
- 批准号:7006656
- 负责人:
- 金额:$ 33.01万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2005
- 资助国家:美国
- 起止时间:2005-02-01 至 2010-01-31
- 项目状态:已结题
- 来源:
- 关键词:AlphavirusRNA biosynthesisRoss River virusSindbis virusVenezuelan equine encephalitis virusbioterrorism /chemical warfareconfocal scanning microscopyhost organism interactionintermolecular interactionlaboratory mouselaboratory rabbitmass spectrometrymolecular assembly /self assemblyprotein localizationprotein structure functionreplicasevirus RNAvirus infection mechanismvirus proteinvirus replication
项目摘要
DESCRIPTION (provided by applicant): Infection of humans and other mammals by members of the Alphavirus genus within the Togaviridae can result in fever, rash, arthritis, encephalitis and death. Several alphaviruses have been designated by the Centers for Disease Control and Prevention as Category B agents of concern for possible use in bioterrorism, and as Priority Pathogens by the NIAID. There is currently no specific treatment available for diseases caused by these pathogens.
We are studying Alphavirus replication with the long-term goal of identifying potential therapeutic targets. Replication of incoming positive-sense genomic RNA, which occurs in membrane-associated complexes containing the viral nonstructural proteins (nsPs), first generates a minus strand copy, followed by new progeny plus strand RNAs. We hypothesize that in addition to known differences in the viral nsP components of the minus and plus strand replicases, that recruitment of different host factors facilitates their disparate functions. We also hypothesize that alphaviruses utilize a common strategy of host factor recruitment to replicate their respective genomes.
Using mutants expressing a tagged nsP3 protein, we propose to use immunological techniques to isolate the plus and minus strand replicases from three representative alphaviruses, Sindbis virus, Ross River virus, and Venezuelan equine encephalitis virus. The host factors present in the replication complexes will be identified by proteomic techniques. Focusing on factors commonly present in the Alphavirus plus and/or minus strand replicase complexes, we will verify each factor's association with the replicase in intact cells using confocal fluorescence microscopy. Using molecular and biochemical approaches, we will assess the effects of associated host components on viral replication and map the protein-protein (or protein-RNA) interactions of the host factors. Understanding the components of and molecular interactions within the Alphavirus minus and plus strand replicases will facilitate future exploration for inhibitors of these important pathogens.
描述(由申请人提供):托加病毒科甲病毒属成员感染人类和其他哺乳动物可导致发烧、皮疹、关节炎、脑炎和死亡。几种甲病毒已被疾病控制和预防中心指定为可能用于生物恐怖主义的B类关注物,并被NIAID指定为优先病原体。目前还没有针对这些病原体引起的疾病的专门治疗方法。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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MARGARET R MACDONALD其他文献
MARGARET R MACDONALD的其他文献
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{{ truncateString('MARGARET R MACDONALD', 18)}}的其他基金
Powassan virus nanobodies from camelid monomeric variable antibody domains elicited by natural infection
自然感染引起的骆驼单体可变抗体域的波瓦桑病毒纳米抗体
- 批准号:
10043364 - 财政年份:2020
- 资助金额:
$ 33.01万 - 项目类别:
Powassan virus nanobodies from camelid monomeric variable antibody domains elicited by natural infection
自然感染引起的骆驼单体可变抗体域的波瓦桑病毒纳米抗体
- 批准号:
10192656 - 财政年份:2020
- 资助金额:
$ 33.01万 - 项目类别:
Genome wide siRNA screen for identifying host factors required for ZAP function
全基因组 siRNA 筛选,用于鉴定 ZAP 功能所需的宿主因子
- 批准号:
8289157 - 财政年份:2012
- 资助金额:
$ 33.01万 - 项目类别:
Upregulation of ZAP expression as a novel approach for anti-alphavirus therapy
ZAP 表达上调作为抗甲病毒治疗的新方法
- 批准号:
8420421 - 财政年份:2012
- 资助金额:
$ 33.01万 - 项目类别:
Upregulation of ZAP expression as a novel approach for anti-alphavirus therapy
ZAP 表达上调作为抗甲病毒治疗的新方法
- 批准号:
8298821 - 财政年份:2012
- 资助金额:
$ 33.01万 - 项目类别:
Genome wide siRNA screen for identifying host factors required for ZAP function
全基因组 siRNA 筛选,用于鉴定 ZAP 功能所需的宿主因子
- 批准号:
8434103 - 财政年份:2012
- 资助金额:
$ 33.01万 - 项目类别:
Host factor DNAJC14 as a novel target for broad spectrum anti-flavivirus activity
宿主因子 DNAJC14 作为广谱抗黄病毒活性的新靶标
- 批准号:
8132747 - 财政年份:2010
- 资助金额:
$ 33.01万 - 项目类别:
Development of a genetically tractable nematode model of alphavirus infection
甲病毒感染的遗传易驯化线虫模型的开发
- 批准号:
7661284 - 财政年份:2009
- 资助金额:
$ 33.01万 - 项目类别:
Development of a genetically tractable nematode model of alphavirus infection
甲病毒感染的遗传易驯化线虫模型的开发
- 批准号:
7764768 - 财政年份:2009
- 资助金额:
$ 33.01万 - 项目类别:
Host factors in the alphavirus replication complex
甲病毒复制复合物中的宿主因子
- 批准号:
7185849 - 财政年份:2005
- 资助金额:
$ 33.01万 - 项目类别:














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