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A modular platform for one-step assembly of multi-component membrane systems by fusion of charged proteoliposomes
An important goal in synthetic biology is the assembly of biomimetic cell-like structures, which combine multiple biological components in synthetic lipid vesicles. A key limiting assembly step is the incorporation of membrane proteins into the lipid bilayer of the vesicles. Here we present a simple...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059690/ https://www.ncbi.nlm.nih.gov/pubmed/27708275 http://dx.doi.org/10.1038/ncomms13025 |
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author | Ishmukhametov, Robert R. Russell, Aidan N. Berry, Richard M. |
author_facet | Ishmukhametov, Robert R. Russell, Aidan N. Berry, Richard M. |
author_sort | Ishmukhametov, Robert R. |
collection | PubMed |
description | An important goal in synthetic biology is the assembly of biomimetic cell-like structures, which combine multiple biological components in synthetic lipid vesicles. A key limiting assembly step is the incorporation of membrane proteins into the lipid bilayer of the vesicles. Here we present a simple method for delivery of membrane proteins into a lipid bilayer within 5 min. Fusogenic proteoliposomes, containing charged lipids and membrane proteins, fuse with oppositely charged bilayers, with no requirement for detergent or fusion-promoting proteins, and deliver large, fragile membrane protein complexes into the target bilayers. We demonstrate the feasibility of our method by assembling a minimal electron transport chain capable of adenosine triphosphate (ATP) synthesis, combining Escherichia coli F(1)F(o) ATP-synthase and the primary proton pump bo(3)-oxidase, into synthetic lipid vesicles with sizes ranging from 100 nm to ∼10 μm. This provides a platform for the combination of multiple sets of membrane protein complexes into cell-like artificial structures. |
format | Online Article Text |
id | pubmed-5059690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50596902016-10-26 A modular platform for one-step assembly of multi-component membrane systems by fusion of charged proteoliposomes Ishmukhametov, Robert R. Russell, Aidan N. Berry, Richard M. Nat Commun Article An important goal in synthetic biology is the assembly of biomimetic cell-like structures, which combine multiple biological components in synthetic lipid vesicles. A key limiting assembly step is the incorporation of membrane proteins into the lipid bilayer of the vesicles. Here we present a simple method for delivery of membrane proteins into a lipid bilayer within 5 min. Fusogenic proteoliposomes, containing charged lipids and membrane proteins, fuse with oppositely charged bilayers, with no requirement for detergent or fusion-promoting proteins, and deliver large, fragile membrane protein complexes into the target bilayers. We demonstrate the feasibility of our method by assembling a minimal electron transport chain capable of adenosine triphosphate (ATP) synthesis, combining Escherichia coli F(1)F(o) ATP-synthase and the primary proton pump bo(3)-oxidase, into synthetic lipid vesicles with sizes ranging from 100 nm to ∼10 μm. This provides a platform for the combination of multiple sets of membrane protein complexes into cell-like artificial structures. Nature Publishing Group 2016-10-06 /pmc/articles/PMC5059690/ /pubmed/27708275 http://dx.doi.org/10.1038/ncomms13025 Text en Copyright © 2016, The Author(s) 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 Ishmukhametov, Robert R. Russell, Aidan N. Berry, Richard M. A modular platform for one-step assembly of multi-component membrane systems by fusion of charged proteoliposomes |
title | A modular platform for one-step assembly of multi-component membrane systems by fusion of charged proteoliposomes |
title_full | A modular platform for one-step assembly of multi-component membrane systems by fusion of charged proteoliposomes |
title_fullStr | A modular platform for one-step assembly of multi-component membrane systems by fusion of charged proteoliposomes |
title_full_unstemmed | A modular platform for one-step assembly of multi-component membrane systems by fusion of charged proteoliposomes |
title_short | A modular platform for one-step assembly of multi-component membrane systems by fusion of charged proteoliposomes |
title_sort | modular platform for one-step assembly of multi-component membrane systems by fusion of charged proteoliposomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059690/ https://www.ncbi.nlm.nih.gov/pubmed/27708275 http://dx.doi.org/10.1038/ncomms13025 |
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