K2P channel gating mechanisms revealed by structures of TREK-2 and a complex with Prozac

Author:

Dong Yin Yao1,Pike Ashley C. W.1,Mackenzie Alexandra12,McClenaghan Conor23,Aryal Prafulla234,Dong Liang1,Quigley Andrew1,Grieben Mariana1,Goubin Solenne1,Mukhopadhyay Shubhashish1,Ruda Gian Filippo15,Clausen Michael V.2,Cao Lishuang6,Brennan Paul E.15,Burgess-Brown Nicola A.1,Sansom Mark S. P.34,Tucker Stephen J.23,Carpenter Elisabeth P.13

Affiliation:

1. Structural Genomics Consortium, University of Oxford, Oxford OX3 7DQ, UK.

2. Clarendon Laboratory, Department of Physics, University of Oxford, Oxford OX1 3PU, UK.

3. OXION Initiative in Ion Channels and Disease, University of Oxford, Oxford OX1 3PN, UK.

4. Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK.

5. Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford OX3 7FZ, UK.

6. Pfizer Neusentis, Granta Park, Cambridge CB21 6GS, UK.

Abstract

A sensitive regulator of cellular potassium A class of potassium channels called K2P channels modulates resting membrane potential in most cells. The channels are regulated by multiple ligands, including the antidepressant drug Prozac, as well as factors such as mechanical stretch and voltage. Dong et al. determined the structure of the human K2P channel, TREK-2, in two conformations and bound to a metabolite of Prozac. The structures show how ligand binding or mechanical stretch might induce switching between the states. Although both states have open channels, one appears primed for gating. A Prozac metabolite binds to the primed state and prevents conformational switching. K2P channels are not a target of Prozac, but their inhibition may contribute to side effects. Science , this issue p. 1256

Funder

Boehringer Ingelheim

Pfizer

Bayer

GlaxoSmithKline

Wellcome Trust

AbbVie

Ontario Genomics Institute

Ontario Ministry of Economic Development and Innovation

UK Biotechnology and Biological Sciences Research Council

Janssen

Lilly Canada

Novartis Research Foundation

Takeda

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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