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Investigation of the defensive mechanisms of HIV-1 Vpu against the antiviral host factor BST-2

Investigation of the defensive mechanisms of HIV-1 Vpu against the antiviral host factor BST-2
HIV-1 Vpu对抗抗病毒宿主因子BST-2防御机制的研究
批准号:
22590428
负责人:
TOKUNAGA Kenzo
金额:
$2.91万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2010
资助国家:
日本
项目状态:
已结题
起止时间:
2010 至 2012

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中文摘要
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英文摘要
HIV-1 Vpu enhances virion production by downregulating the antiviral host factor BST-2 from the cell surface. In this study, we attempted to identify host cofactors that play a supporting role in the anti-BST-2 activity of Vpu. We first prepared Vpu-binding proteins by performing immunoprecipitation assay, and identified multiple candidate proteins by proteome analyses. The candidate proteins were cloned into expression plasmids and then co-expressed with Vpu, followed by immunoprecipitation and subcellular localization assays. Knocking-down the gene expression of the candidate proteins that proved to interact with and colocalize with Vpu revealed no effect on Vpu’s anti-BST-2 activity, implying that those proteins might be involved in other functions of Vpu.
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DOI: --
发表时间: 2011
期刊:
影响因子: --
作者: [藤田英明, 岩部幸枝, 佐多徹太郎, 徳永研三, 田中嘉孝]
通讯作者: 田中嘉孝
HIV-1 integraion into host DNA double-strand break sites is the majority event in integrase inhibitor-treated cells
HIV-1 整合到宿主 DNA 双链断裂位点是整合酶抑制剂处理的细胞中的主要事件
DOI: --
发表时间: 2011
期刊:
影响因子: --
作者: [Takayoshi Koyama, Kenzo Tokunaga, Yukihito Ishizaka]
通讯作者: Yukihito Ishizaka
Site-Specific Integration of a Lentiviral Vector in the Human Genome via DNA Double-Strand Breaks.
通过 DNA 双链断裂将慢病毒载体定点整合到人类基因组中。
DOI: --
发表时间: 2010
期刊:
影响因子: --
作者: [Takayoshi Koyama, Kenzo Tokunaga, Tetsutaro Sata, Yukihito Ishizaka]
通讯作者: Yukihito Ishizaka
DOI: 10.1186/1742-4690-10-21
发表时间: 2013-02-21
期刊: Retrovirology
影响因子: 3.3
作者: [Koyama T, Sun B, Tokunaga K, Tatsumi M, Ishizaka Y]
通讯作者: Ishizaka Y
65
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