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
相关论文
共 50 条
  • [41] Localization of TREK-2 K+ channel domains that regulate channel kinetics and sensitivity to pressure, fatty acids and pHi
    Kim, Y
    Gnatenco, C
    Bang, H
    Kim, D
    PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2001, 442 (06): : 952 - 960
  • [42] Localization of TREK-2 K+ channel domains that regulate channel kinetics and sensitivity to pressure, fatty acids and pHi
    Yangmi Kim
    Carmen Gnatenco
    Hyoweon Bang
    Donghee Kim
    Pflügers Archiv, 2001, 442 : 952 - 960
  • [43] A nanobody toolkit for the regulation of K2P channel function
    Tucker, Stephen J.
    BIOPHYSICAL JOURNAL, 2023, 122 (03) : 294A - 294A
  • [44] Identification of the large-conductance background K+ channel in mouse B cells as TREK-2
    Zheng, Haifeng
    Nam, Joo Hyun
    Pang, Bo
    Shin, Dong Hoon
    Kim, Ji Seon
    Chun, Yang-Sook
    Park, Jong-Wan
    Bang, Hyowon
    Kim, Woo Kyung
    Earm, Yung E.
    Kim, Sung Joon
    AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2009, 297 (01): : C188 - C197
  • [45] Identification of Gating Mutations in the Trek-1 k2p Potassium Channel by Functional Complementation in K plus uptake Deficient Yeast
    Sharma, Chetan
    Bollepalli, Murali K.
    Baukrowitz, Thomas
    Tucker, Stephen J.
    BIOPHYSICAL JOURNAL, 2011, 100 (03) : 279 - 280
  • [46] Molecular mechanisms of activation in K2P potassium channels
    Baukrowitz, T.
    ACTA PHYSIOLOGICA, 2019, 227
  • [47] A mutation in the selectivity filter of the K2P channel TREK-1 causes right ventricular outflow tract tachycardia
    Bonnin, B. Ortiz
    Friedrich, C.
    Zumhagen, S.
    Rinne, S.
    Stallmeyer, B.
    Schulze-Bahr, E.
    Decher, N.
    ACTA PHYSIOLOGICA, 2014, 210 : 62 - 62
  • [48] Cross-talk between the mechano-gated K2P channel TREK-1 and the actin cytoskeleton
    Lauritzen, I
    Chemin, J
    Honoré, E
    Jodar, M
    Guy, N
    Lazdunski, M
    Patel, AJ
    EMBO REPORTS, 2005, 6 (07) : 642 - 648
  • [49] Prognostic significance of the TREK-1 K2P potassium channels in prostate cancer
    Zhang, Gui-Ming
    Wan, Fang-Ning
    Qin, Xiao-Jian
    Cao, Da-Long
    Zhang, Hai-Liang
    Zhu, Yao
    Dai, Bo
    Shi, Guo-Hai
    Ye, Ding-Wei
    ONCOTARGET, 2015, 6 (21) : 18460 - 18468
  • [50] TREK-2 (K2P10.1) and TRESK (K2P18.1) are major background K+ channels in dorsal root ganglion neurons
    Kang, Dawon
    Kim, Donghee
    AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2006, 291 (01): : C138 - C146