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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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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 |
format | Online Article Text |
id | pubmed-3925968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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