Development of high sensitivity antibody protein chip using tagged antibody produced by genetic recombination technology.
Project/Area Number |
25460689
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Laboratory medicine
|
Research Institution | Yamaguchi University |
Principal Investigator |
FURUMOTO Hiroko 山口大学, 医学(系)研究科(研究院), 講師 (70311818)
|
Project Period (FY) |
2013-04-01 – 2017-03-31
|
Project Status |
Completed (Fiscal Year 2016)
|
Budget Amount *help |
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
|
Keywords | 蛋白チップ / 抗体開発 / タンパクチップ |
Outline of Final Research Achievements |
An antibody chip is a tool used to exhaustively analyze protein expression in full detail. The purpose of this study is to create a new technology for antibody arrays by developing a highly sensitive next generation antibody chip, using the technology where a tagged protein is immobilized on a diamond-like surface treated substrate. Thus, we created a monoclonal antibody where the tag-sequence was added to immunoglobulin G (IgG) using genetic recombination technology. The tag introduced IgG and a control IgG were produced in a cell culture system. Then, they were fixed to the substrate to evaluate the state of the antibody and antigen-detection efficiency on the substrate with or without the tag. As a result, it was confirmed that a tagged-antibodies are high sensitivity, but hundreds of different kind of tagged-antibodies are required for the creation of the antibody array. Therefore, a high-throughput production system of the tagged-antibody, such as genome editing is under trial.
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Report
(5 results)
Research Products
(1 results)