| Project/Area Number |
16360119
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Intelligent mechanics/Mechanical systems
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| Research Institution | The University of Tokyo |
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Principal Investigator |
SUZUKI Hiroaki The University of Tokyo, Institute of Industrial Science, Research Associate, 生産技術研究所, 助手 (20372427)
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| Co-Investigator(Kenkyū-buntansha) |
NOJI Hiroyuki Osaka University, The Institute of Scientific and Industrial Research, Professor, 産業科学研究所, 教授 (00343111)
TAKEUCHI Shoji The University of Tokyo, Institute of Industrial Science, Associate Professor, 生産技術研究所, 助教授 (90343110)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥13,400,000 (Direct Cost: ¥13,400,000)
Fiscal Year 2005: ¥3,800,000 (Direct Cost: ¥3,800,000)
Fiscal Year 2004: ¥9,600,000 (Direct Cost: ¥9,600,000)
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| Keywords | Mirco / Nano Fabrication Technology / Array Chip / Membrane Protein / Planar Lipid Bilayer |
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| Research Abstract |
We developed a highly reproducible method for planar lipid bilayer reconstitution using a micro-fluidic system made of a polymethyl methacrylate (PMMA) plastic substrate. Planar lipid bilayers are formed at apertures, 100 μm diameter, by flowing lipid solution and buffer alternately into an integrated micro-fluidic channel. Since the amount and distribution of the lipid solution at the aperture determines the state of the lipid bilayer, controlling them precisely is crucial. We designed the geometry of the fluidic system so that a constant amount of lipid solution is distributed at the aperture. Then, the layer of lipid solution is thinned by applying an external pressure, and finally becomes a bilayer when a pressure of 200-400 Pa is applied. The formation process can be simultaneously monitored with optical and electric recordings. The maximum yield for bilayer formation was 90%. Using this technique, four lipid bilayers are formed simultaneously in a single chip. Finally, a channel current through gramicidin peptide ion channels are recorded to prove the compatibility of the chip with single molecule electrophysiology.
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