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Lipid Driven Nanodomains in Giant Lipid Vesicles are Fluid and Disordered
It is a fundamental question in cell biology and biophysics whether sphingomyelin (SM)- and cholesterol (Chol)- driven nanodomains exist in living cells and in model membranes. Biophysical studies on model membranes revealed SM and Chol driven micrometer-sized liquid-ordered domains. Although the ex...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511215/ https://www.ncbi.nlm.nih.gov/pubmed/28710349 http://dx.doi.org/10.1038/s41598-017-05539-y |
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author | Koukalová, Alena Amaro, Mariana Aydogan, Gokcan Gröbner, Gerhard Williamson, Philip T. F. Mikhalyov, Ilya Hof, Martin Šachl, Radek |
author_facet | Koukalová, Alena Amaro, Mariana Aydogan, Gokcan Gröbner, Gerhard Williamson, Philip T. F. Mikhalyov, Ilya Hof, Martin Šachl, Radek |
author_sort | Koukalová, Alena |
collection | PubMed |
description | It is a fundamental question in cell biology and biophysics whether sphingomyelin (SM)- and cholesterol (Chol)- driven nanodomains exist in living cells and in model membranes. Biophysical studies on model membranes revealed SM and Chol driven micrometer-sized liquid-ordered domains. Although the existence of such microdomains has not been proven for the plasma membrane, such lipid mixtures have been often used as a model system for ‘rafts’. On the other hand, recent super resolution and single molecule results indicate that the plasma membrane might organize into nanocompartments. However, due to the limited resolution of those techniques their unambiguous characterization is still missing. In this work, a novel combination of Förster resonance energy transfer and Monte Carlo simulations (MC-FRET) identifies directly 10 nm large nanodomains in liquid-disordered model membranes composed of lipid mixtures containing SM and Chol. Combining MC-FRET with solid-state wide-line and high resolution magic angle spinning NMR as well as with fluorescence correlation spectroscopy we demonstrate that these nanodomains containing hundreds of lipid molecules are fluid and disordered. In terms of their size, fluidity, order and lifetime these nanodomains may represent a relevant model system for cellular membranes and are closely related to nanocompartments suggested to exist in cellular membranes. |
format | Online Article Text |
id | pubmed-5511215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55112152017-07-17 Lipid Driven Nanodomains in Giant Lipid Vesicles are Fluid and Disordered Koukalová, Alena Amaro, Mariana Aydogan, Gokcan Gröbner, Gerhard Williamson, Philip T. F. Mikhalyov, Ilya Hof, Martin Šachl, Radek Sci Rep Article It is a fundamental question in cell biology and biophysics whether sphingomyelin (SM)- and cholesterol (Chol)- driven nanodomains exist in living cells and in model membranes. Biophysical studies on model membranes revealed SM and Chol driven micrometer-sized liquid-ordered domains. Although the existence of such microdomains has not been proven for the plasma membrane, such lipid mixtures have been often used as a model system for ‘rafts’. On the other hand, recent super resolution and single molecule results indicate that the plasma membrane might organize into nanocompartments. However, due to the limited resolution of those techniques their unambiguous characterization is still missing. In this work, a novel combination of Förster resonance energy transfer and Monte Carlo simulations (MC-FRET) identifies directly 10 nm large nanodomains in liquid-disordered model membranes composed of lipid mixtures containing SM and Chol. Combining MC-FRET with solid-state wide-line and high resolution magic angle spinning NMR as well as with fluorescence correlation spectroscopy we demonstrate that these nanodomains containing hundreds of lipid molecules are fluid and disordered. In terms of their size, fluidity, order and lifetime these nanodomains may represent a relevant model system for cellular membranes and are closely related to nanocompartments suggested to exist in cellular membranes. Nature Publishing Group UK 2017-07-14 /pmc/articles/PMC5511215/ /pubmed/28710349 http://dx.doi.org/10.1038/s41598-017-05539-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Koukalová, Alena Amaro, Mariana Aydogan, Gokcan Gröbner, Gerhard Williamson, Philip T. F. Mikhalyov, Ilya Hof, Martin Šachl, Radek Lipid Driven Nanodomains in Giant Lipid Vesicles are Fluid and Disordered |
title | Lipid Driven Nanodomains in Giant Lipid Vesicles are Fluid and Disordered |
title_full | Lipid Driven Nanodomains in Giant Lipid Vesicles are Fluid and Disordered |
title_fullStr | Lipid Driven Nanodomains in Giant Lipid Vesicles are Fluid and Disordered |
title_full_unstemmed | Lipid Driven Nanodomains in Giant Lipid Vesicles are Fluid and Disordered |
title_short | Lipid Driven Nanodomains in Giant Lipid Vesicles are Fluid and Disordered |
title_sort | lipid driven nanodomains in giant lipid vesicles are fluid and disordered |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511215/ https://www.ncbi.nlm.nih.gov/pubmed/28710349 http://dx.doi.org/10.1038/s41598-017-05539-y |
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