Pharmacology of voltage-gated and calcium-activated potassium channels

被引:130
作者
Kaczorowski, GJ [1 ]
Garcia, ML [1 ]
机构
[1] Merck Res Labs, Dept Membrane Biochem & Biophys, Rahway, NJ 07065 USA
关键词
D O I
10.1016/S1367-5931(99)80066-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several important new findings have furthered the development of voltage-gated and calcium-activated potassium channel pharmacology. The molecular constituents of several members of these large ion channel families were identified. Small-molecule modulators of some of these channels were reported, including correolide, the first potent, small-molecule, natural product inhibitor of the Shaker family of voltage-gated potassium channels to be disclosed. The initial crystal structure of a bacterial potassium channel was determined; this work gives a physical basis for understanding the mechanisms of ion selectivity and ion conduction. With the recent molecular characterization of a potassium channel structure and the discovery of new templates for channel modulatory agents, the ability to rationally identify and develop potassium channel agonists and antagonists may become a reality in the near future.
引用
收藏
页码:448 / 458
页数:11
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