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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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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. |
format | Online Article Text |
id | pubmed-8186909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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