| Project/Area Number |
23770222
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Multi-year Fund |
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| Research Field |
Cell biology
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| Research Institution | Mie University |
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Principal Investigator |
TSUMOTO Kanta 三重大学, 大学院・工学研究科, 講師 (80362359)
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| Project Period (FY) |
2011 – 2012
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| Project Status |
Completed (Fiscal Year 2012)
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| Budget Amount *help |
¥3,250,000 (Direct Cost: ¥2,500,000、Indirect Cost: ¥750,000)
Fiscal Year 2012: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2011: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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| Keywords | 人工細胞モデル / 巨大リポソーム / シグナル伝達 / 膜タンパク質再構成 / バキュロウイルス / GUV(Giant Unilamellar Vesicle) / 少数要素による構成実験 / 細胞情報 / GUV |
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| Research Abstract |
Membrane protein components were incorporated into membranes of giant liposomes (giant unilamellar vesicles, GUVs) by fusing recombinant baculovirus budded virus (BV) envelope particles that displayed (or expressed) the target membrane proteins with membranes of the giant liposomes. In this study, we tried to constitute a classical and fundamental pathway of signal transduction from three kinds of membrane proteins (G-protein coupled receptor, GPCR; G protein; adenylate cyclase, ADCY). The incorporation of single polypeptides of these proteins was observed using a confocal laser scanning microscope on a single GUV level. On the other hand, however, we were faced with a problem to be solved as to reproducibility of biochemical assay of signal transduction (production of cAMP). For promotion of the study related to artificial cell systems, we also successfully developed a novel experimental procedure based on single giant liposomes.
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