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Single molecule FRET reveals pore size and opening mechanism of a mechano-sensitive ion channel

The mechanosensitive channel of large conductance, which serves as a model system for mechanosensitive channels, has previously been crystallized in the closed form, but not in the open form. Ensemble measurements and electrophysiological sieving experiments show that the open-diameter of the channe...

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Autores principales: Wang, Yong, Liu, Yanxin, DeBerg, Hannah A, Nomura, Takeshi, Hoffman, Melinda Tonks, Rohde, Paul R, Schulten, Klaus, Martinac, Boris, Selvin, Paul R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925968/
https://www.ncbi.nlm.nih.gov/pubmed/24550255
http://dx.doi.org/10.7554/eLife.01834
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author Wang, Yong
Liu, Yanxin
DeBerg, Hannah A
Nomura, Takeshi
Hoffman, Melinda Tonks
Rohde, Paul R
Schulten, Klaus
Martinac, Boris
Selvin, Paul R
author_facet Wang, Yong
Liu, Yanxin
DeBerg, Hannah A
Nomura, Takeshi
Hoffman, Melinda Tonks
Rohde, Paul R
Schulten, Klaus
Martinac, Boris
Selvin, Paul R
author_sort Wang, Yong
collection PubMed
description The mechanosensitive channel of large conductance, which serves as a model system for mechanosensitive channels, has previously been crystallized in the closed form, but not in the open form. Ensemble measurements and electrophysiological sieving experiments show that the open-diameter of the channel pore is >25 Å, but the exact size and whether the conformational change follows a helix-tilt or barrel-stave model are unclear. Here we report measurements of the distance changes on liposome-reconstituted MscL transmembrane α-helices, using a ‘virtual sorting’ single-molecule fluorescence energy transfer. We observed directly that the channel opens via the helix-tilt model and the open pore reaches 2.8 nm in diameter. In addition, based on the measurements, we developed a molecular dynamics model of the channel structure in the open state which confirms our direct observations. DOI: http://dx.doi.org/10.7554/eLife.01834.001
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spelling pubmed-39259682014-02-27 Single molecule FRET reveals pore size and opening mechanism of a mechano-sensitive ion channel Wang, Yong Liu, Yanxin DeBerg, Hannah A Nomura, Takeshi Hoffman, Melinda Tonks Rohde, Paul R Schulten, Klaus Martinac, Boris Selvin, Paul R eLife Biophysics and Structural Biology The mechanosensitive channel of large conductance, which serves as a model system for mechanosensitive channels, has previously been crystallized in the closed form, but not in the open form. Ensemble measurements and electrophysiological sieving experiments show that the open-diameter of the channel pore is >25 Å, but the exact size and whether the conformational change follows a helix-tilt or barrel-stave model are unclear. Here we report measurements of the distance changes on liposome-reconstituted MscL transmembrane α-helices, using a ‘virtual sorting’ single-molecule fluorescence energy transfer. We observed directly that the channel opens via the helix-tilt model and the open pore reaches 2.8 nm in diameter. In addition, based on the measurements, we developed a molecular dynamics model of the channel structure in the open state which confirms our direct observations. DOI: http://dx.doi.org/10.7554/eLife.01834.001 eLife Sciences Publications, Ltd 2014-02-18 /pmc/articles/PMC3925968/ /pubmed/24550255 http://dx.doi.org/10.7554/eLife.01834 Text en Copyright © 2014, Wang et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biophysics and Structural Biology
Wang, Yong
Liu, Yanxin
DeBerg, Hannah A
Nomura, Takeshi
Hoffman, Melinda Tonks
Rohde, Paul R
Schulten, Klaus
Martinac, Boris
Selvin, Paul R
Single molecule FRET reveals pore size and opening mechanism of a mechano-sensitive ion channel
title Single molecule FRET reveals pore size and opening mechanism of a mechano-sensitive ion channel
title_full Single molecule FRET reveals pore size and opening mechanism of a mechano-sensitive ion channel
title_fullStr Single molecule FRET reveals pore size and opening mechanism of a mechano-sensitive ion channel
title_full_unstemmed Single molecule FRET reveals pore size and opening mechanism of a mechano-sensitive ion channel
title_short Single molecule FRET reveals pore size and opening mechanism of a mechano-sensitive ion channel
title_sort single molecule fret reveals pore size and opening mechanism of a mechano-sensitive ion channel
topic Biophysics and Structural Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925968/
https://www.ncbi.nlm.nih.gov/pubmed/24550255
http://dx.doi.org/10.7554/eLife.01834
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