FEBS Letters | |
The structure, function and distribution of the mouse TWIK‐1 K+ channel | |
Lazdunski, Michel1  Lesage, Florian1  Reyes, Roberto1  Duprat, Fabrice1  Heurteaux, Catherine1  Fink, Michel1  Lauritzen, Inger1  | |
[1] Institut de Pharmacologie Moléculaire et Cellulaire, CNRS, 660, route des Lucioles, Sophia Antipolis, 06560 Valbonne, France | |
关键词: Heterologous expression; Xenopus oocyte; In situ hybridization; Two P domains; | |
DOI : 10.1016/S0014-5793(96)01491-3 | |
学科分类:生物化学/生物物理 | |
来源: John Wiley & Sons Ltd. | |
【 摘 要 】
The two P domain K+ channel mTWIK-1 has been cloned from mouse brain. In Xenopus oocytes, mTWIK-1 currents are K+-selective, instantaneous, and weakly inward rectifying. These currents are blocked by Ba2+ and quinine, decreased by protein kinase C and increased by internal acidification. The apparent molecular weight of mTWIK-1 in brain is 81 kDa. A 40 kDa form is revealed after treatment with a reducing agent, strongly suggesting that native mTWIK-1 subunits dimerize via a disulfide bridge. TWIK-1 mRNA is expressed abundantly in brain and at lower levels in lung, kidney, and skeletal muscle. In situ hybridization shows that mTWIK-1 expression is restricted to a few brain regions, with the highest levels in cerebellar granule cells, brainstem, hippocampus and cerebral cortex.
【 授权许可】
Unknown
【 预 览 】
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RO201912020303868ZK.pdf | 552KB | download |