| Project/Area Number |
26620134
|
|---|
| Research Category |
Grant-in-Aid for Challenging Exploratory Research
|
| Allocation Type | Multi-year Fund |
|---|
| Research Field |
Bio-related chemistry
|
|---|
| Research Institution | Kyoto University |
|---|
Principal Investigator |
NAKATA EIJI 京都大学, エネルギー理工学研究所, 講師 (70467827)
|
|---|
| Project Period (FY) |
2014-04-01 – 2016-03-31
|
| Project Status |
Completed (Fiscal Year 2015)
|
| Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Fiscal Year 2014: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
|
|---|
| Keywords | バイオセンサー / 蛍光 / 構造変化 / リガンド / リセプタータンパク質 / レシオ検出 |
|---|
| Outline of Final Research Achievements |
Genetically encoded fluorescent biosensor proteins offer the possibility to probe the concentration of key metabolites in living cells. The approaches currently used to generate such fluorescent biosensor proteins lack generality, as they require a protein that undergoes a conformational change upon ligand binding. In this research, we try an approach that overcomes this limitation. Our biosensor consist of receptor protein for ligand, fluorescent protein and ligand mimicked peptide. In the presence of the ligand of interest, the ligand displaces the ligand mimicked peptide, thereby inducing spectral change. On the other hands, the control-biosensor, which did not have the ligand mimicked peptide, could not sense the ligand of interest because the conformational change was not induced. These results clearly indicated that our strategy was useful to construct fluorescent biosensor.
|
