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动态双联体:Kir6 和 SUR 在 K 通道结构和功能中的作用。

Dynamic duo: Kir6 and SUR in K channel structure and function.

机构信息

Department of Chemical Physiology and Biochemistry, School of Medicine, Oregon Health and Science University, Portland, OR, USA.

Department of Medical Biochemistry, Tanta University, Tanta, Egypt.

出版信息

Channels (Austin). 2024 Dec;18(1):2327708. doi: 10.1080/19336950.2024.2327708. Epub 2024 Mar 15.

Abstract

K channels are ligand-gated potassium channels that couple cellular energetics with membrane potential to regulate cell activity. Each channel is an eight subunit complex comprising four central pore-forming Kir6 inward rectifier potassium channel subunits surrounded by four regulatory subunits known as the sulfonylurea receptor, SUR, which confer homeostatic metabolic control of K gating. SUR is an ATP binding cassette (ABC) protein family homolog that lacks membrane transport activity but is essential for K expression and function. For more than four decades, understanding the structure-function relationship of Kir6 and SUR has remained a central objective of clinical significance. Here, we review progress in correlating the wealth of functional data in the literature with recent K cryoEM structures.

摘要

K 通道是配体门控钾通道,它将细胞能量与膜电位偶联起来,以调节细胞活动。每个通道都是由四个中央孔形成的 Kir6 内向整流钾通道亚基组成的八亚基复合物,周围环绕着四个称为磺酰脲受体(SUR)的调节亚基,该受体赋予 K 门控的同源代谢控制。SUR 是 ATP 结合盒(ABC)蛋白家族同源物,它缺乏膜转运活性,但对 K 的表达和功能至关重要。四十多年来,理解 Kir6 和 SUR 的结构-功能关系一直是具有临床意义的核心目标。在这里,我们回顾了将文献中丰富的功能数据与最近的 K 冷冻电镜结构相关联的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ba/10950283/faa7bb6f01ec/KCHL_A_2327708_F0001_OC.jpg

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