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磺脲类受体/内向整流钾通道6.X(sur/KIR6.X),即ATP敏感性钾通道的示意图。

A view of sur/KIR6.X, KATP channels.

作者信息

Babenko A P, Aguilar-Bryan L, Bryan J

机构信息

Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Annu Rev Physiol. 1998;60:667-87. doi: 10.1146/annurev.physiol.60.1.667.

Abstract

ATP-sensitive potassium channels, termed KATP channels, link the electrical activity of cell membranes to cellular metabolism. These channels are heteromultimers of sulfonylurea receptor (SUR) and KIR6.X subunits associated with a 1:1 stoichiometry as a tetramer (SUR/KIR6.X forms the pores, whereas SUR regulates their activity. Changes in [ATP]i and [ADP]i gate the channel. The diversity of KATP channels results from the assembly of SUR and KIR6.X subtypes KIR6.1-based channels differ from KIR6.2 channels mainly by their smaller unitary conductance. SUR1- and SUR2-based channels are distinguished by their differential sensitivity to sulfonylureas, whereas SUR2A-based channels are distinguished from SUR2B channels by their differential sensitivity to diazoxide. Mutations that result in the loss of KATP channels in pancreatic beta-cells have been identified in SUR1 and KIR6.2. These mutations lead to familial hyperinsulinism. Understanding the mutations in SUR and KIR6.X is allowing insight into how these channels respond to nucleotides, sulfonylureas, and potassium channel openers, KCOs.

摘要

ATP敏感性钾通道,称为KATP通道,将细胞膜的电活动与细胞代谢联系起来。这些通道是磺脲类受体(SUR)和KIR6.X亚基的异源多聚体,以1:1的化学计量比形成四聚体(SUR/KIR6.X形成孔道,而SUR调节其活性)。细胞内ATP([ATP]i)和二磷酸腺苷([ADP]i)的变化控制着通道的开闭。KATP通道的多样性源于SUR和KIR6.X亚型的组合。基于KIR6.1的通道与KIR6.2通道的主要区别在于其较小的单位电导。基于SUR1和SUR2的通道通过它们对磺脲类药物的不同敏感性来区分,而基于SUR2A的通道与SUR2B通道的区别在于它们对二氮嗪的不同敏感性。在SUR1和KIR6.2中已鉴定出导致胰腺β细胞中KATP通道功能丧失的突变。这些突变导致家族性高胰岛素血症。了解SUR和KIR6.X中的突变有助于深入了解这些通道如何对核苷酸、磺脲类药物和钾通道开放剂(KCOs)作出反应。

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