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Bilayer-Mediated Structural Transitions Control Mechanosensitivity of the TREK-2 K2P Channel
The mechanosensitive two-pore domain (K2P) K(+) channels (TREK-1, TREK-2, and TRAAK) are important for mechanical and thermal nociception. However, the mechanisms underlying their gating by membrane stretch remain controversial. Here we use molecular dynamics simulations to examine their behavior in...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415359/ https://www.ncbi.nlm.nih.gov/pubmed/28392258 http://dx.doi.org/10.1016/j.str.2017.03.006 |
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author | Aryal, Prafulla Jarerattanachat, Viwan Clausen, Michael V. Schewe, Marcus McClenaghan, Conor Argent, Liam Conrad, Linus J. Dong, Yin Y. Pike, Ashley C.W. Carpenter, Elisabeth P. Baukrowitz, Thomas Sansom, Mark S.P. Tucker, Stephen J. |
author_facet | Aryal, Prafulla Jarerattanachat, Viwan Clausen, Michael V. Schewe, Marcus McClenaghan, Conor Argent, Liam Conrad, Linus J. Dong, Yin Y. Pike, Ashley C.W. Carpenter, Elisabeth P. Baukrowitz, Thomas Sansom, Mark S.P. Tucker, Stephen J. |
author_sort | Aryal, Prafulla |
collection | PubMed |
description | The mechanosensitive two-pore domain (K2P) K(+) channels (TREK-1, TREK-2, and TRAAK) are important for mechanical and thermal nociception. However, the mechanisms underlying their gating by membrane stretch remain controversial. Here we use molecular dynamics simulations to examine their behavior in a lipid bilayer. We show that TREK-2 moves from the “down” to “up” conformation in direct response to membrane stretch, and examine the role of the transmembrane pressure profile in this process. Furthermore, we show how state-dependent interactions with lipids affect the movement of TREK-2, and how stretch influences both the inner pore and selectivity filter. Finally, we present functional studies that demonstrate why direct pore block by lipid tails does not represent the principal mechanism of mechanogating. Overall, this study provides a dynamic structural insight into K2P channel mechanosensitivity and illustrates how the structure of a eukaryotic mechanosensitive ion channel responds to changes in forces within the bilayer. |
format | Online Article Text |
id | pubmed-5415359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54153592017-05-10 Bilayer-Mediated Structural Transitions Control Mechanosensitivity of the TREK-2 K2P Channel Aryal, Prafulla Jarerattanachat, Viwan Clausen, Michael V. Schewe, Marcus McClenaghan, Conor Argent, Liam Conrad, Linus J. Dong, Yin Y. Pike, Ashley C.W. Carpenter, Elisabeth P. Baukrowitz, Thomas Sansom, Mark S.P. Tucker, Stephen J. Structure Article The mechanosensitive two-pore domain (K2P) K(+) channels (TREK-1, TREK-2, and TRAAK) are important for mechanical and thermal nociception. However, the mechanisms underlying their gating by membrane stretch remain controversial. Here we use molecular dynamics simulations to examine their behavior in a lipid bilayer. We show that TREK-2 moves from the “down” to “up” conformation in direct response to membrane stretch, and examine the role of the transmembrane pressure profile in this process. Furthermore, we show how state-dependent interactions with lipids affect the movement of TREK-2, and how stretch influences both the inner pore and selectivity filter. Finally, we present functional studies that demonstrate why direct pore block by lipid tails does not represent the principal mechanism of mechanogating. Overall, this study provides a dynamic structural insight into K2P channel mechanosensitivity and illustrates how the structure of a eukaryotic mechanosensitive ion channel responds to changes in forces within the bilayer. Cell Press 2017-05-02 /pmc/articles/PMC5415359/ /pubmed/28392258 http://dx.doi.org/10.1016/j.str.2017.03.006 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Aryal, Prafulla Jarerattanachat, Viwan Clausen, Michael V. Schewe, Marcus McClenaghan, Conor Argent, Liam Conrad, Linus J. Dong, Yin Y. Pike, Ashley C.W. Carpenter, Elisabeth P. Baukrowitz, Thomas Sansom, Mark S.P. Tucker, Stephen J. Bilayer-Mediated Structural Transitions Control Mechanosensitivity of the TREK-2 K2P Channel |
title | Bilayer-Mediated Structural Transitions Control Mechanosensitivity of the TREK-2 K2P Channel |
title_full | Bilayer-Mediated Structural Transitions Control Mechanosensitivity of the TREK-2 K2P Channel |
title_fullStr | Bilayer-Mediated Structural Transitions Control Mechanosensitivity of the TREK-2 K2P Channel |
title_full_unstemmed | Bilayer-Mediated Structural Transitions Control Mechanosensitivity of the TREK-2 K2P Channel |
title_short | Bilayer-Mediated Structural Transitions Control Mechanosensitivity of the TREK-2 K2P Channel |
title_sort | bilayer-mediated structural transitions control mechanosensitivity of the trek-2 k2p channel |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415359/ https://www.ncbi.nlm.nih.gov/pubmed/28392258 http://dx.doi.org/10.1016/j.str.2017.03.006 |
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