Establishment of novel anti-virus strategy targeting HIV-1 RNA psi pseudoknot.
Project/Area Number |
25460567
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Virology
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Research Institution | Osaka University |
Principal Investigator |
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Project Period (FY) |
2013-04-01 – 2016-03-31
|
Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
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Keywords | HIV-1 / RNA / ウイルスゲノム / パッケージング / 二量体化 / HIV / Gag / 感染 / ウイルス / HIV / ゲノムパッケージング / 偽結節構造 |
Outline of Final Research Achievements |
The genome of HIV-1 always forms dimer in virion. The genome dimerization is believed to have important roles on viral infectivity and/or pathogenicity. Previously I suggested the dimerization signal region RNA (DLS) of HIV-1 forms pseudoknot-like structure. In this project, I explored a precise functional structures around the pseudoknot, such as SL1 and primer binding site applying virological/molecular biological approach. In addition, I focused on the p1 region, which is important for viral maturation process and examined its roles on viral infectivity and genome packaging. .
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Report
(4 results)
Research Products
(16 results)
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[Journal Article] Fibrocytes differ from macrophages but can be infected with HIV-1.2015
Author(s)
M. Hashimoto, H. Nasser, F. Bhuyan, N. Kuse, Y. Satou, S. Harada, K. Yoshimura, J. Sakuragi, K. Monde, Y. Maeda, S. Welbourn, K. Strebel, E.W.A. El-Wahab, M. Miyazaki , S. Hattori, N. Chutiwitoonchai, M. Hiyoshi, S. Oka, M. Takiguchi, S. Suzu.
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Journal Title
The Journal of Immunology
Volume: 195
Issue: 9
Pages: 4341-4350
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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