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内向整流型ATP调节钾通道的克隆与表达

Cloning and expression of an inwardly rectifying ATP-regulated potassium channel.

作者信息

Ho K, Nichols C G, Lederer W J, Lytton J, Vassilev P M, Kanazirska M V, Hebert S C

机构信息

Harvard Center for the Study of Kidney Disease, Harvard Medical School, Boston, Massachusetts.

出版信息

Nature. 1993 Mar 4;362(6415):31-8. doi: 10.1038/362031a0.

Abstract

A complementary DNA encoding an ATP-regulated potassium channel has been isolated by expression cloning from rat kidney. The predicted 45K protein, which features two potential membrane-spanning helices and a proposed ATP-binding domain, represents a major departure from the basic structural design characteristic of voltage-gated and second messenger-gated ion channels. But the presence of an H5 region, which is likely to form the ion conduction pathway, indicates that the protein may share a common origin with voltage-gated potassium channel proteins.

摘要

通过从大鼠肾脏进行表达克隆,已分离出一种编码ATP调节钾通道的互补DNA。预测的45K蛋白具有两个潜在的跨膜螺旋和一个推测的ATP结合结构域,这与电压门控和第二信使门控离子通道的基本结构设计特征有很大不同。但是存在一个可能形成离子传导途径的H5区域,这表明该蛋白可能与电压门控钾通道蛋白有共同的起源。

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