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

Abstract:
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.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1085/jgp.201611601

Authors


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Role:
Author
ORCID:
0000-0002-0859-3854
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Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
NDM; Structural Genomics Consortium
Role:
Author


Publisher:
Rockefeller University Press
Journal:
Journal of General Physiology More from this journal
Volume:
147
Issue:
6
Pages:
497-505
Publication date:
2016-05-01
Acceptance date:
2016-05-09
DOI:
EISSN:
1540-7748
ISSN:
0022-1295
Pmid:
27241700


Language:
English
Keywords:
Pubs id:
pubs:625393
UUID:
uuid:a609ef5a-ea28-4658-a668-e396b0836ab0
Local pid:
pubs:625393
Source identifiers:
625393
Deposit date:
2018-03-26

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