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Order vs. Disorder: Cholesterol and Omega-3 Phospholipids Determine Biomembrane Organization
Lipid structural diversity strongly affects biomembrane chemico-physical and structural properties in addition to membrane-associated events. At high concentrations, cholesterol increases membrane order and rigidity, while polyunsaturated lipids are reported to increase disorder and flexibility. How...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140907/ https://www.ncbi.nlm.nih.gov/pubmed/35628128 http://dx.doi.org/10.3390/ijms23105322 |
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author | de Santis, Augusta Scoppola, Ernesto Ottaviani, Maria Francesca Koutsioubas, Alexandros Barnsley, Lester C. Paduano, Luigi D’Errico, Gerardino Russo Krauss, Irene |
author_facet | de Santis, Augusta Scoppola, Ernesto Ottaviani, Maria Francesca Koutsioubas, Alexandros Barnsley, Lester C. Paduano, Luigi D’Errico, Gerardino Russo Krauss, Irene |
author_sort | de Santis, Augusta |
collection | PubMed |
description | Lipid structural diversity strongly affects biomembrane chemico-physical and structural properties in addition to membrane-associated events. At high concentrations, cholesterol increases membrane order and rigidity, while polyunsaturated lipids are reported to increase disorder and flexibility. How these different tendencies balance in composite bilayers is still controversial. In this study, electron paramagnetic resonance spectroscopy, small angle neutron scattering, and neutron reflectivity were used to investigate the structural properties of cholesterol-containing lipid bilayers in the fluid state with increasing amounts of polyunsaturated omega-3 lipids. Either the hybrid 1-stearoyl-2-docosahexaenoyl-sn-glycero-3-phosphocholine or the symmetric 1,2-docosahexaenoyl-sn-glycero-3-phosphocholine were added to the mixture of the naturally abundant 1-palmitoyl-2-oleyl-sn-glycero-3-phosphocholine and cholesterol. Our results indicate that the hybrid and the symmetric omega-3 phospholipids affect the microscopic organization of lipid bilayers differently. Cholesterol does not segregate from polyunsaturated phospholipids and, through interactions with them, is able to suppress the formation of non-lamellar structures induced by the symmetric polyunsaturated lipid. However, this order/disorder balance leads to a bilayer whose structural organization cannot be ascribed to either a liquid ordered or to a canonical liquid disordered phase, in that it displays a very loose packing of the intermediate segments of lipid chains. |
format | Online Article Text |
id | pubmed-9140907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91409072022-05-28 Order vs. Disorder: Cholesterol and Omega-3 Phospholipids Determine Biomembrane Organization de Santis, Augusta Scoppola, Ernesto Ottaviani, Maria Francesca Koutsioubas, Alexandros Barnsley, Lester C. Paduano, Luigi D’Errico, Gerardino Russo Krauss, Irene Int J Mol Sci Article Lipid structural diversity strongly affects biomembrane chemico-physical and structural properties in addition to membrane-associated events. At high concentrations, cholesterol increases membrane order and rigidity, while polyunsaturated lipids are reported to increase disorder and flexibility. How these different tendencies balance in composite bilayers is still controversial. In this study, electron paramagnetic resonance spectroscopy, small angle neutron scattering, and neutron reflectivity were used to investigate the structural properties of cholesterol-containing lipid bilayers in the fluid state with increasing amounts of polyunsaturated omega-3 lipids. Either the hybrid 1-stearoyl-2-docosahexaenoyl-sn-glycero-3-phosphocholine or the symmetric 1,2-docosahexaenoyl-sn-glycero-3-phosphocholine were added to the mixture of the naturally abundant 1-palmitoyl-2-oleyl-sn-glycero-3-phosphocholine and cholesterol. Our results indicate that the hybrid and the symmetric omega-3 phospholipids affect the microscopic organization of lipid bilayers differently. Cholesterol does not segregate from polyunsaturated phospholipids and, through interactions with them, is able to suppress the formation of non-lamellar structures induced by the symmetric polyunsaturated lipid. However, this order/disorder balance leads to a bilayer whose structural organization cannot be ascribed to either a liquid ordered or to a canonical liquid disordered phase, in that it displays a very loose packing of the intermediate segments of lipid chains. MDPI 2022-05-10 /pmc/articles/PMC9140907/ /pubmed/35628128 http://dx.doi.org/10.3390/ijms23105322 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article de Santis, Augusta Scoppola, Ernesto Ottaviani, Maria Francesca Koutsioubas, Alexandros Barnsley, Lester C. Paduano, Luigi D’Errico, Gerardino Russo Krauss, Irene Order vs. Disorder: Cholesterol and Omega-3 Phospholipids Determine Biomembrane Organization |
title | Order vs. Disorder: Cholesterol and Omega-3 Phospholipids Determine Biomembrane Organization |
title_full | Order vs. Disorder: Cholesterol and Omega-3 Phospholipids Determine Biomembrane Organization |
title_fullStr | Order vs. Disorder: Cholesterol and Omega-3 Phospholipids Determine Biomembrane Organization |
title_full_unstemmed | Order vs. Disorder: Cholesterol and Omega-3 Phospholipids Determine Biomembrane Organization |
title_short | Order vs. Disorder: Cholesterol and Omega-3 Phospholipids Determine Biomembrane Organization |
title_sort | order vs. disorder: cholesterol and omega-3 phospholipids determine biomembrane organization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140907/ https://www.ncbi.nlm.nih.gov/pubmed/35628128 http://dx.doi.org/10.3390/ijms23105322 |
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