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Kir 通道的分子生理学、药理学及治疗学意义。

Kir Channel Molecular Physiology, Pharmacology, and Therapeutic Implications.

机构信息

Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Bouvé College of Health Sciences, Northeastern University, Boston, MA, USA.

Department of Chemistry and Chemical Biology, College of Science, Northeastern University, Boston, MA, USA.

出版信息

Handb Exp Pharmacol. 2021;267:277-356. doi: 10.1007/164_2021_501.

Abstract

For the past two decades several scholarly reviews have appeared on the inwardly rectifying potassium (Kir) channels. We would like to highlight two efforts in particular, which have provided comprehensive reviews of the literature up to 2010 (Hibino et al., Physiol Rev 90(1):291-366, 2010; Stanfield et al., Rev Physiol Biochem Pharmacol 145:47-179, 2002). In the past decade, great insights into the 3-D atomic resolution structures of Kir channels have begun to provide the molecular basis for their functional properties. More recently, computational studies are beginning to close the time domain gap between in silico dynamic and patch-clamp functional studies. The pharmacology of these channels has also been expanding and the dynamic structural studies provide hope that we are heading toward successful structure-based drug design for this family of K channels. In the present review we focus on placing the physiology and pharmacology of this K channel family in the context of atomic resolution structures and in providing a glimpse of the promising future of therapeutic opportunities.

摘要

在过去的二十年中,出现了几篇关于内向整流钾 (Kir) 通道的学术综述。我们特别想强调两项努力,它们对截至 2010 年的文献进行了全面综述(Hibino 等人,《生理学评论》90(1):291-366, 2010;Stanfield 等人,《生理学、生物化学和药理学评论》145:47-179, 2002)。在过去的十年中,对 Kir 通道的三维原子分辨率结构的深入了解开始为其功能特性提供了分子基础。最近,计算研究开始缩小计算动态和膜片钳功能研究之间的时间域差距。这些通道的药理学也在不断扩展,动态结构研究有望为这一系列 K 通道的基于结构的药物设计带来成功。在本综述中,我们重点介绍了该 K 通道家族的生理学和药理学在原子分辨率结构中的背景,并提供了治疗机会的有希望的未来一瞥。

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