Molecular basis for the cation-chloride co-transporter activity
| Project/Area Number |
23590301
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Multi-year Fund |
|---|
| Section | 一般 |
|---|
| Research Field |
General pharmacology
|
|---|
| Research Institution | Osaka University |
|---|
Principal Investigator |
INANOBE Atsushi 大阪大学, 医学(系)研究科(研究院), 准教授 (00270851)
|
|---|
| Project Period (FY) |
2011 – 2013
|
| Project Status |
Completed (Fiscal Year 2013)
|
| Budget Amount *help |
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2011: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
|
|---|
| Keywords | 膜イオン輸送体 / 再構成実験系 / 構造機能相関 / 疾患関連遺伝子 / イオン輸送体 / リポソーム再構成系 |
|---|
| Research Abstract |
The ion transport across cell membranes is essential for a survival of all types of cells. This cellular function is mediated by various ion channels and transporters. These molecular machineries are targets for many therapeutic drugs for hypertension and diabetes. Cation-chloride co-transporters transport Na+, K+ and Cl-, but there is no net charge for one transport cycle across membranes. This manner of the activity is electroneutral, and makes it difficult to assess the activity, the drug-interaction and the effect of inherited mutations in detail. In this study, we tried to develop the reconstitution system for a prokaryotic CCC homologue to liposomes. However, although the homologue possesses properties suit for biochemical analyses, it was totally difficult to control its protein expression. Instead of this approach, we succeeded to develop a cell-based platform as the conventional method to analyze this transporter.
|
Report
(4 results)
Research Products
(61 results)
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
[Journal Article] A mechanism underlying compound-induced voltage shift in the current activation of hERG by antiarrhythmic agents2011
Author(s)
Furutani, K., Yamakawa, Y., Inanobe, A., Iwata, M., Ohno, Y., Kurachi, Y.
-
Journal Title
A mechanism underlying compound-induced voltage shift in the current activation of hERG by antiarrhythmic agents
Volume: 415(1)
Issue: 1
Pages: 141-146
DOI
Related Report
Peer Reviewed
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
