Molecular Mechanism of Poxvirus Host Range Genes
Molecular Mechanism of Poxvirus Host Range Genes
批准号:
7196807
负责人:
YAN XIANG
金额:
$21.9万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-20 至 2009-08-31
关键词:
Amino Acid Sequence HomologyAnkyrin RepeatAntiviral AgentsCell LineCell physiologyCellsDevelopmentGenesGenomeGrowthHumanIn VitroKnowledgeMAPK7 geneMediatingMitogen-Activated Protein KinasesMolecularMonkeypox virusOrthopoxvirusPoxviridaeProteinsRangeSmallpox VirusesStructureSurfaceTestingVaccinia virusViralVirulencebasehuman MAP kinase 7mouse modelnovel vaccinesprotein protein interaction
中文摘要
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英文摘要
DESCRIPTION: Orthopoxviruses can replicate productively in a very broad range of cell lines in vitro, but their replications in some specific cell lines are abortive unless the so-called "host-range" genes are intact in their genome [1]. In our preliminary studies, a functional host-range gene, either K1L or C7L or CP77, was found to be also required for vaccinia virus (W) to replicate productively in primary human cells and for W virulence in a mouse model. However, the mechanisms by which these host-range genes support viral growth in otherwise non-permissive host are not clear. K1L, C7L and CP77 share no significant amino acid sequence homology, but both CP77 and K1L encode multiple ankyrin repeats. Because ankyrin repeats proteins typically function in mediating specific protein-protein interactions [2, 3], we hypothesize that CP77 and K1L interact with specific viral or/and cellular factors via their ankyrin repeats to circumvent some intracellular barriers of poxvirus replication. This hypothesis is supported by our preliminary studies that demonstrated: (1) variable surface residues of a few consecutive K1L ankyrin repeats are essential for its host-range function in human cells;(2) K1L interacts with W C10L protein during viral replication; and (3) K1L interacts directly with extracellular signal-regulated kinase 5 (ERK5), a crucial component of mitogen- activated protein kinase (MAPK) cascades regulating multiple cellular processes. We will further test our hypothesis by accomplishing the following specific aims: 1. To explore the molecular basis for the host-range function through structure-function analysis ofK1LandCP77. 2. To determine whether K1L mediates its host-range function through interactions with ERK5 . and WCIOL Accomplishing these two specific aims will provide some fundamental knowledge about the intracellular barriers of orthopoxviral replication and viral strategies of circumventing these barriers. This will benefit the development of safer vaccines and novel antivirals for pathogenic Orthopoxviruses such as variola virus and monkeypox virus.
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批准号:8632750
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资助金额:$38.4万
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资助金额:$33.3万
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批准号:7690939
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资助金额:$33.41万
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Immune modulation mechanism mediated by poxvirus IL-18 binding protein
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批准号:7901593
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资助金额:$33.41万
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Poxvirus Immune Evasion Mechanisms
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资助金额:$37.17万
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财政年份:2008
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负责人:YAN XIANG
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Immune modulation mechanism mediated by poxvirus IL-18 binding protein
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批准号:8133520
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项目类别:
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资助金额:$33.08万
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财政年份:2008
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负责人:YAN XIANG
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依托单位:
Molecular Mechanism of Poxvirus Host Range Genes
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批准号:7497488
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项目类别:
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资助金额:$17.9万
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财政年份:2007
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负责人:YAN XIANG
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依托单位:
Poxvirus immune modulators and the host Immune system
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批准号:6719620
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项目类别:
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资助金额:$10.8万
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财政年份:2003
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依托单位:
Poxvirus immune modulators and the host Immune system
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批准号:6558913
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项目类别:
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资助金额:$16.2万
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财政年份:2003
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依托单位:
海外基金