Polymodal activation of the TREK-2 K2P channel produces structurally distinct open states

被引:58
|
作者
McClenaghan, Conor [1 ,2 ]
Schewe, Marcus [4 ]
Aryal, Prafulla [1 ,2 ]
Carpenter, Elisabeth P. [2 ,3 ]
Baukrowitz, Thomas [4 ]
Tucker, Stephen J. [1 ,2 ]
机构
[1] Univ Oxford, Dept Phys, Clarendon Lab, Oxford OX1 3PU, England
[2] Univ Oxford, OXION Initiat Ion Channels & Dis, Oxford OX1 3PU, England
[3] Univ Oxford, Struct Genom Consortium, Oxford OX3 7DQ, England
[4] Univ Kiel, Dept Physiol, Olshaussenstr 40, D-24118 Kiel, Germany
来源
JOURNAL OF GENERAL PHYSIOLOGY | 2016年 / 147卷 / 06期
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
K+ CHANNELS; POTASSIUM CHANNEL; FATTY-ACIDS; TRAAK; LEAK; K-2P; SENSITIVITY; MECHANISM; PRESSURE; CRYSTAL;
D O I
10.1085/jgp.201611601
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The TREK subfamily of two-pore domain (K2P) K+ channels exhibit polymodal gating by a wide range of physical and chemical stimuli. Crystal structures now exist for these channels in two main states referred to as the "up" and "down" conformations. However, recent studies have resulted in contradictory and mutually exclusive conclusions about the functional (i.e., conductive) status of these two conformations. To address this problem, we have used the state-dependent TREK-2 inhibitor norfluoxetine that can only bind to the down state, thereby allowing us to distinguish between these two conformations when activated by different stimuli. Our results reconcile these previously contradictory gating models by demonstrating that activation by pressure, temperature, voltage, and pH produce more than one structurally distinct open state and reveal that channel activation does not simply involve switching between the up and down conformations. These results also highlight the diversity of structural mechanisms that K2P channels use to integrate polymodal gating signals.
引用
收藏
页码:497 / 505
页数:9
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