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The push-to-open mechanism of the tethered mechanosensitive ion channel NompC

NompC is a mechanosensitive ion channel responsible for the sensation of touch and balance in Drosophila melanogaster. Based on a resolved cryo-EM structure, we performed all-atom molecular dynamics simulations and electrophysiological experiments to study the atomistic details of NompC gating. Our...

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Detalles Bibliográficos
Autores principales: Wang, Yang, Guo, Yifeng, Li, Guanluan, Liu, Chunhong, Wang, Lei, Zhang, Aihua, Yan, Zhiqiang, Song, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186909/
https://www.ncbi.nlm.nih.gov/pubmed/34101577
http://dx.doi.org/10.7554/eLife.58388
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author Wang, Yang
Guo, Yifeng
Li, Guanluan
Liu, Chunhong
Wang, Lei
Zhang, Aihua
Yan, Zhiqiang
Song, Chen
author_facet Wang, Yang
Guo, Yifeng
Li, Guanluan
Liu, Chunhong
Wang, Lei
Zhang, Aihua
Yan, Zhiqiang
Song, Chen
author_sort Wang, Yang
collection PubMed
description NompC is a mechanosensitive ion channel responsible for the sensation of touch and balance in Drosophila melanogaster. Based on a resolved cryo-EM structure, we performed all-atom molecular dynamics simulations and electrophysiological experiments to study the atomistic details of NompC gating. Our results showed that NompC could be opened by compression of the intracellular ankyrin repeat domain but not by a stretch, and a number of hydrogen bonds along the force convey pathway are important for the mechanosensitivity. Under intracellular compression, the bundled ankyrin repeat region acts like a spring with a spring constant of ~13 pN nm(−1) by transferring forces at a rate of ~1.8 nm ps(−1). The linker helix region acts as a bridge between the ankyrin repeats and the transient receptor potential (TRP) domain, which passes on the pushing force to the TRP domain to undergo a clockwise rotation, resulting in the opening of the channel. This could be the universal gating mechanism of similar tethered mechanosensitive TRP channels, which enable cells to feel compression and shrinkage.
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spelling pubmed-81869092021-06-09 The push-to-open mechanism of the tethered mechanosensitive ion channel NompC Wang, Yang Guo, Yifeng Li, Guanluan Liu, Chunhong Wang, Lei Zhang, Aihua Yan, Zhiqiang Song, Chen eLife Computational and Systems Biology NompC is a mechanosensitive ion channel responsible for the sensation of touch and balance in Drosophila melanogaster. Based on a resolved cryo-EM structure, we performed all-atom molecular dynamics simulations and electrophysiological experiments to study the atomistic details of NompC gating. Our results showed that NompC could be opened by compression of the intracellular ankyrin repeat domain but not by a stretch, and a number of hydrogen bonds along the force convey pathway are important for the mechanosensitivity. Under intracellular compression, the bundled ankyrin repeat region acts like a spring with a spring constant of ~13 pN nm(−1) by transferring forces at a rate of ~1.8 nm ps(−1). The linker helix region acts as a bridge between the ankyrin repeats and the transient receptor potential (TRP) domain, which passes on the pushing force to the TRP domain to undergo a clockwise rotation, resulting in the opening of the channel. This could be the universal gating mechanism of similar tethered mechanosensitive TRP channels, which enable cells to feel compression and shrinkage. eLife Sciences Publications, Ltd 2021-06-08 /pmc/articles/PMC8186909/ /pubmed/34101577 http://dx.doi.org/10.7554/eLife.58388 Text en © 2021, Wang et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Wang, Yang
Guo, Yifeng
Li, Guanluan
Liu, Chunhong
Wang, Lei
Zhang, Aihua
Yan, Zhiqiang
Song, Chen
The push-to-open mechanism of the tethered mechanosensitive ion channel NompC
title The push-to-open mechanism of the tethered mechanosensitive ion channel NompC
title_full The push-to-open mechanism of the tethered mechanosensitive ion channel NompC
title_fullStr The push-to-open mechanism of the tethered mechanosensitive ion channel NompC
title_full_unstemmed The push-to-open mechanism of the tethered mechanosensitive ion channel NompC
title_short The push-to-open mechanism of the tethered mechanosensitive ion channel NompC
title_sort push-to-open mechanism of the tethered mechanosensitive ion channel nompc
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186909/
https://www.ncbi.nlm.nih.gov/pubmed/34101577
http://dx.doi.org/10.7554/eLife.58388
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