Advanced hybridoma technology for generating next generation of therapeutic medicines
| Project/Area Number |
24360339
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Partial Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Biofunction/Bioprocess
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| Research Institution | Mie University |
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Principal Investigator |
Tomita Masahiro 三重大学, 工学(系)研究科(研究院), 教授 (20183494)
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| Co-Investigator(Kenkyū-buntansha) |
MIZUTANI Fumio 兵庫県立大学, 大学院物質理学研究科, 教授 (80118603)
YASUKAWA Tomoyuki 兵庫県立大学, 大学院物質理学研究科, 准教授 (40361167)
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| Project Period (FY) |
2012-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥19,240,000 (Direct Cost: ¥14,800,000、Indirect Cost: ¥4,440,000)
Fiscal Year 2014: ¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2013: ¥5,850,000 (Direct Cost: ¥4,500,000、Indirect Cost: ¥1,350,000)
Fiscal Year 2012: ¥8,580,000 (Direct Cost: ¥6,600,000、Indirect Cost: ¥1,980,000)
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| Keywords | B細胞 / 抗原発現細胞 / ハイブリドーマ / 立体構造特異的抗体 / 誘電泳動 / 細胞配列 / 免疫捕捉 / 細胞分離 |
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| Outline of Final Research Achievements |
B cells harboring aimed specific antigen-receptors were captured by antigen-expressing myeloma cells and selectively fused by electrical pulses to generate hybridoma cells secreting stereospecific monoclonal antibodies. By using this method, hybridoma cells can be fabricated to produce the stereospecific structure of the specific receptors on the cell membrane. Cell manipulation technique based on the dielectrophoresis was utilized to introduce the cells to the microwell array electrode and form single cell pairs with different types of cells rapidly and simply. Thus, the use of the present dielectrophoretic manipulation allows large numbers of cell pairs (over 100,000 pairs) to be produced within only 1 min.
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Report
(5 results)
Research Products
(268 results)
