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Asymmetric Hybrid Polymer–Lipid Giant Vesicles as Cell Membrane Mimics
Lipid membrane asymmetry plays an important role in cell function and activity, being for instance a relevant signal of its integrity. The development of artificial asymmetric membranes thus represents a key challenge. In this context, an emulsion‐centrifugation method is developed to prepare giant...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770682/ https://www.ncbi.nlm.nih.gov/pubmed/29375971 http://dx.doi.org/10.1002/advs.201700453 |
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author | Peyret, Ariane Ibarboure, Emmanuel Le Meins, Jean‐François Lecommandoux, Sebastien |
author_facet | Peyret, Ariane Ibarboure, Emmanuel Le Meins, Jean‐François Lecommandoux, Sebastien |
author_sort | Peyret, Ariane |
collection | PubMed |
description | Lipid membrane asymmetry plays an important role in cell function and activity, being for instance a relevant signal of its integrity. The development of artificial asymmetric membranes thus represents a key challenge. In this context, an emulsion‐centrifugation method is developed to prepare giant vesicles with an asymmetric membrane composed of an inner monolayer of poly(butadiene)‐b‐poly(ethylene oxide) (PBut‐b‐PEO) and outer monolayer of 1‐palmitoyl‐2‐oleoyl‐sn‐glycero‐3‐phosphocholine (POPC). The formation of a complete membrane asymmetry is demonstrated and its stability with time is followed by measuring lipid transverse diffusion. From fluorescence spectroscopy measurements, the lipid half‐life is estimated to be 7.5 h. Using fluorescence recovery after photobleaching technique, the diffusion coefficient of 1,2‐dioleoyl‐sn‐glycero‐3‐phosphoethanolamine‐N‐(lissamine rhodamine B sulfonyl) (DOPE‐rhod, inserted into the POPC leaflet) is determined to be about D = 1.8 ± 0.50 μm(2) s(−1) at 25 °C and D = 2.3 ± 0.7 μm(2) s(−1) at 37 °C, between the characteristic values of pure POPC and pure polymer giant vesicles and in good agreement with the diffusion of lipids in a variety of biological membranes. These results demonstrate the ability to prepare a cell‐like model system that displays an asymmetric membrane with transverse and translational diffusion properties similar to that of biological cells. |
format | Online Article Text |
id | pubmed-5770682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57706822018-01-26 Asymmetric Hybrid Polymer–Lipid Giant Vesicles as Cell Membrane Mimics Peyret, Ariane Ibarboure, Emmanuel Le Meins, Jean‐François Lecommandoux, Sebastien Adv Sci (Weinh) Full Papers Lipid membrane asymmetry plays an important role in cell function and activity, being for instance a relevant signal of its integrity. The development of artificial asymmetric membranes thus represents a key challenge. In this context, an emulsion‐centrifugation method is developed to prepare giant vesicles with an asymmetric membrane composed of an inner monolayer of poly(butadiene)‐b‐poly(ethylene oxide) (PBut‐b‐PEO) and outer monolayer of 1‐palmitoyl‐2‐oleoyl‐sn‐glycero‐3‐phosphocholine (POPC). The formation of a complete membrane asymmetry is demonstrated and its stability with time is followed by measuring lipid transverse diffusion. From fluorescence spectroscopy measurements, the lipid half‐life is estimated to be 7.5 h. Using fluorescence recovery after photobleaching technique, the diffusion coefficient of 1,2‐dioleoyl‐sn‐glycero‐3‐phosphoethanolamine‐N‐(lissamine rhodamine B sulfonyl) (DOPE‐rhod, inserted into the POPC leaflet) is determined to be about D = 1.8 ± 0.50 μm(2) s(−1) at 25 °C and D = 2.3 ± 0.7 μm(2) s(−1) at 37 °C, between the characteristic values of pure POPC and pure polymer giant vesicles and in good agreement with the diffusion of lipids in a variety of biological membranes. These results demonstrate the ability to prepare a cell‐like model system that displays an asymmetric membrane with transverse and translational diffusion properties similar to that of biological cells. John Wiley and Sons Inc. 2017-12-05 /pmc/articles/PMC5770682/ /pubmed/29375971 http://dx.doi.org/10.1002/advs.201700453 Text en © 2017 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Peyret, Ariane Ibarboure, Emmanuel Le Meins, Jean‐François Lecommandoux, Sebastien Asymmetric Hybrid Polymer–Lipid Giant Vesicles as Cell Membrane Mimics |
title | Asymmetric Hybrid Polymer–Lipid Giant Vesicles as Cell Membrane Mimics |
title_full | Asymmetric Hybrid Polymer–Lipid Giant Vesicles as Cell Membrane Mimics |
title_fullStr | Asymmetric Hybrid Polymer–Lipid Giant Vesicles as Cell Membrane Mimics |
title_full_unstemmed | Asymmetric Hybrid Polymer–Lipid Giant Vesicles as Cell Membrane Mimics |
title_short | Asymmetric Hybrid Polymer–Lipid Giant Vesicles as Cell Membrane Mimics |
title_sort | asymmetric hybrid polymer–lipid giant vesicles as cell membrane mimics |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770682/ https://www.ncbi.nlm.nih.gov/pubmed/29375971 http://dx.doi.org/10.1002/advs.201700453 |
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