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Activation of bacterial channel MscL in mechanically stimulated droplet interface bilayers
MscL, a stretch-activated channel, saves bacteria experiencing hypo-osmotic shocks from lysis. Its high conductance and controllable activation makes it a strong candidate to serve as a transducer in stimuli-responsive biomolecular materials. Droplet interface bilayers (DIBs), flexible insulating sc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562232/ https://www.ncbi.nlm.nih.gov/pubmed/26348441 http://dx.doi.org/10.1038/srep13726 |
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author | Najem, Joseph S. Dunlap, Myles D. Rowe, Ian D. Freeman, Eric C. Grant, John W. Sukharev, Sergei Leo, Donald J. |
author_facet | Najem, Joseph S. Dunlap, Myles D. Rowe, Ian D. Freeman, Eric C. Grant, John W. Sukharev, Sergei Leo, Donald J. |
author_sort | Najem, Joseph S. |
collection | PubMed |
description | MscL, a stretch-activated channel, saves bacteria experiencing hypo-osmotic shocks from lysis. Its high conductance and controllable activation makes it a strong candidate to serve as a transducer in stimuli-responsive biomolecular materials. Droplet interface bilayers (DIBs), flexible insulating scaffolds for such materials, can be used as a new platform for incorporation and activation of MscL. Here, we report the first reconstitution and activation of the low-threshold V23T mutant of MscL in a DIB as a response to axial compressions of the droplets. Gating occurs near maximum compression of both droplets where tension in the membrane is maximal. The observed 0.1–3 nS conductance levels correspond to the V23T-MscL sub-conductive and fully open states recorded in native bacterial membranes or liposomes. Geometrical analysis of droplets during compression indicates that both contact angle and total area of the water-oil interfaces contribute to the generation of tension in the bilayer. The measured expansion of the interfaces by 2.5% is predicted to generate a 4–6 mN/m tension in the bilayer, just sufficient for gating. This work clarifies the principles of interconversion between bulk and surface forces in the DIB, facilitates the measurements of fundamental membrane properties, and improves our understanding of MscL response to membrane tension. |
format | Online Article Text |
id | pubmed-4562232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45622322015-09-15 Activation of bacterial channel MscL in mechanically stimulated droplet interface bilayers Najem, Joseph S. Dunlap, Myles D. Rowe, Ian D. Freeman, Eric C. Grant, John W. Sukharev, Sergei Leo, Donald J. Sci Rep Article MscL, a stretch-activated channel, saves bacteria experiencing hypo-osmotic shocks from lysis. Its high conductance and controllable activation makes it a strong candidate to serve as a transducer in stimuli-responsive biomolecular materials. Droplet interface bilayers (DIBs), flexible insulating scaffolds for such materials, can be used as a new platform for incorporation and activation of MscL. Here, we report the first reconstitution and activation of the low-threshold V23T mutant of MscL in a DIB as a response to axial compressions of the droplets. Gating occurs near maximum compression of both droplets where tension in the membrane is maximal. The observed 0.1–3 nS conductance levels correspond to the V23T-MscL sub-conductive and fully open states recorded in native bacterial membranes or liposomes. Geometrical analysis of droplets during compression indicates that both contact angle and total area of the water-oil interfaces contribute to the generation of tension in the bilayer. The measured expansion of the interfaces by 2.5% is predicted to generate a 4–6 mN/m tension in the bilayer, just sufficient for gating. This work clarifies the principles of interconversion between bulk and surface forces in the DIB, facilitates the measurements of fundamental membrane properties, and improves our understanding of MscL response to membrane tension. Nature Publishing Group 2015-09-08 /pmc/articles/PMC4562232/ /pubmed/26348441 http://dx.doi.org/10.1038/srep13726 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Najem, Joseph S. Dunlap, Myles D. Rowe, Ian D. Freeman, Eric C. Grant, John W. Sukharev, Sergei Leo, Donald J. Activation of bacterial channel MscL in mechanically stimulated droplet interface bilayers |
title | Activation of bacterial channel MscL in mechanically stimulated droplet interface bilayers |
title_full | Activation of bacterial channel MscL in mechanically stimulated droplet interface bilayers |
title_fullStr | Activation of bacterial channel MscL in mechanically stimulated droplet interface bilayers |
title_full_unstemmed | Activation of bacterial channel MscL in mechanically stimulated droplet interface bilayers |
title_short | Activation of bacterial channel MscL in mechanically stimulated droplet interface bilayers |
title_sort | activation of bacterial channel mscl in mechanically stimulated droplet interface bilayers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562232/ https://www.ncbi.nlm.nih.gov/pubmed/26348441 http://dx.doi.org/10.1038/srep13726 |
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