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Directly imaging emergence of phase separation in peroxidized lipid membranes

Lipid peroxidation is a process which is key in cell signaling and disease, it is exploited in cancer therapy in the form of photodynamic therapy. The appearance of hydrophilic moieties within the bilayer’s hydrocarbon core will dramatically alter the structure and mechanical behavior of membranes....

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Autores principales: Paez-Perez, Miguel, Vyšniauskas, Aurimas, López-Duarte, Ismael, Lafarge, Eulalie J., López-Ríos De Castro, Raquel, Marques, Carlos M., Schroder, André P., Muller, Pierre, Lorenz, Christian D., Brooks, Nicholas J., Kuimova, Marina K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845225/
https://www.ncbi.nlm.nih.gov/pubmed/36697756
http://dx.doi.org/10.1038/s42004-022-00809-x
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author Paez-Perez, Miguel
Vyšniauskas, Aurimas
López-Duarte, Ismael
Lafarge, Eulalie J.
López-Ríos De Castro, Raquel
Marques, Carlos M.
Schroder, André P.
Muller, Pierre
Lorenz, Christian D.
Brooks, Nicholas J.
Kuimova, Marina K.
author_facet Paez-Perez, Miguel
Vyšniauskas, Aurimas
López-Duarte, Ismael
Lafarge, Eulalie J.
López-Ríos De Castro, Raquel
Marques, Carlos M.
Schroder, André P.
Muller, Pierre
Lorenz, Christian D.
Brooks, Nicholas J.
Kuimova, Marina K.
author_sort Paez-Perez, Miguel
collection PubMed
description Lipid peroxidation is a process which is key in cell signaling and disease, it is exploited in cancer therapy in the form of photodynamic therapy. The appearance of hydrophilic moieties within the bilayer’s hydrocarbon core will dramatically alter the structure and mechanical behavior of membranes. Here, we combine viscosity sensitive fluorophores, advanced microscopy, and X-ray diffraction and molecular simulations to directly and quantitatively measure the bilayer’s structural and viscoelastic properties, and correlate these with atomistic molecular modelling. Our results indicate an increase in microviscosity and a decrease in the bending rigidity upon peroxidation of the membranes, contrary to the trend observed with non-oxidized lipids. Fluorescence lifetime imaging microscopy and MD simulations give evidence for the presence of membrane regions of different local order in the oxidized membranes. We hypothesize that oxidation promotes stronger lipid-lipid interactions, which lead to an increase in the lateral heterogeneity within the bilayer and the creation of lipid clusters of higher order.
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spelling pubmed-98452252023-01-19 Directly imaging emergence of phase separation in peroxidized lipid membranes Paez-Perez, Miguel Vyšniauskas, Aurimas López-Duarte, Ismael Lafarge, Eulalie J. López-Ríos De Castro, Raquel Marques, Carlos M. Schroder, André P. Muller, Pierre Lorenz, Christian D. Brooks, Nicholas J. Kuimova, Marina K. Commun Chem Article Lipid peroxidation is a process which is key in cell signaling and disease, it is exploited in cancer therapy in the form of photodynamic therapy. The appearance of hydrophilic moieties within the bilayer’s hydrocarbon core will dramatically alter the structure and mechanical behavior of membranes. Here, we combine viscosity sensitive fluorophores, advanced microscopy, and X-ray diffraction and molecular simulations to directly and quantitatively measure the bilayer’s structural and viscoelastic properties, and correlate these with atomistic molecular modelling. Our results indicate an increase in microviscosity and a decrease in the bending rigidity upon peroxidation of the membranes, contrary to the trend observed with non-oxidized lipids. Fluorescence lifetime imaging microscopy and MD simulations give evidence for the presence of membrane regions of different local order in the oxidized membranes. We hypothesize that oxidation promotes stronger lipid-lipid interactions, which lead to an increase in the lateral heterogeneity within the bilayer and the creation of lipid clusters of higher order. Nature Publishing Group UK 2023-01-17 /pmc/articles/PMC9845225/ /pubmed/36697756 http://dx.doi.org/10.1038/s42004-022-00809-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Paez-Perez, Miguel
Vyšniauskas, Aurimas
López-Duarte, Ismael
Lafarge, Eulalie J.
López-Ríos De Castro, Raquel
Marques, Carlos M.
Schroder, André P.
Muller, Pierre
Lorenz, Christian D.
Brooks, Nicholas J.
Kuimova, Marina K.
Directly imaging emergence of phase separation in peroxidized lipid membranes
title Directly imaging emergence of phase separation in peroxidized lipid membranes
title_full Directly imaging emergence of phase separation in peroxidized lipid membranes
title_fullStr Directly imaging emergence of phase separation in peroxidized lipid membranes
title_full_unstemmed Directly imaging emergence of phase separation in peroxidized lipid membranes
title_short Directly imaging emergence of phase separation in peroxidized lipid membranes
title_sort directly imaging emergence of phase separation in peroxidized lipid membranes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845225/
https://www.ncbi.nlm.nih.gov/pubmed/36697756
http://dx.doi.org/10.1038/s42004-022-00809-x
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