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Domain Size Regulation in Phospholipid Model Membranes Using Oil Molecules and Hybrid Lipids

[Image: see text] The formation of domains in multicomponent lipid mixtures has been suggested to play a role in moderating signal transduction in cells. Understanding how domain size may be regulated by both hybrid lipid molecules and impurities is important for understanding real biological proces...

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Autores principales: Scheidegger, Laura, Stricker, Laura, Beltramo, Peter J., Vermant, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9377339/
https://www.ncbi.nlm.nih.gov/pubmed/35895895
http://dx.doi.org/10.1021/acs.jpcb.2c02862
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author Scheidegger, Laura
Stricker, Laura
Beltramo, Peter J.
Vermant, Jan
author_facet Scheidegger, Laura
Stricker, Laura
Beltramo, Peter J.
Vermant, Jan
author_sort Scheidegger, Laura
collection PubMed
description [Image: see text] The formation of domains in multicomponent lipid mixtures has been suggested to play a role in moderating signal transduction in cells. Understanding how domain size may be regulated by both hybrid lipid molecules and impurities is important for understanding real biological processes; at the same time, developing model systems where domain size can be regulated is crucial to enable systematic studies of domain formation kinetics and thermodynamics. Here, we perform a model study of the effects of oil molecules, which swell the bilayer, and line-active hybrid phospholipids using a thermally induced liquid–solid phase separation in planar, free-standing lipid bilayers consisting of DOPC and DPPC (1,2-dioleoyl-sn-glycero-3-phosphocholine and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine, respectively). The experiments show that the kinetics of domain growth are significantly affected by the type and molecular structure of the oil (squalene, hexadecane, or decane), with the main contributing factors being the degree of swelling of the bilayer and the changes in line tension induced by the different oils, with smaller domains resulting from systems with smaller values of the line tension. POPC (1-palmitoyl-sn-2-oleoyl-glycero-3-phosphocholine), on the other hand, acts as a line-active hybrid lipid, reducing the domain size when added in small amounts and slowing down domain coarsening. Finally, we show that despite the regulation of domain size by both methods, the phase transition temperature is influenced by the presence of oil molecules but not significantly by the presence of hybrid lipids. Overall, our results show how to regulate domain size in binary membrane model systems, over a wide range of length scales, by incorporating oil molecules and hybrid lipids.
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spelling pubmed-93773392023-07-27 Domain Size Regulation in Phospholipid Model Membranes Using Oil Molecules and Hybrid Lipids Scheidegger, Laura Stricker, Laura Beltramo, Peter J. Vermant, Jan J Phys Chem B [Image: see text] The formation of domains in multicomponent lipid mixtures has been suggested to play a role in moderating signal transduction in cells. Understanding how domain size may be regulated by both hybrid lipid molecules and impurities is important for understanding real biological processes; at the same time, developing model systems where domain size can be regulated is crucial to enable systematic studies of domain formation kinetics and thermodynamics. Here, we perform a model study of the effects of oil molecules, which swell the bilayer, and line-active hybrid phospholipids using a thermally induced liquid–solid phase separation in planar, free-standing lipid bilayers consisting of DOPC and DPPC (1,2-dioleoyl-sn-glycero-3-phosphocholine and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine, respectively). The experiments show that the kinetics of domain growth are significantly affected by the type and molecular structure of the oil (squalene, hexadecane, or decane), with the main contributing factors being the degree of swelling of the bilayer and the changes in line tension induced by the different oils, with smaller domains resulting from systems with smaller values of the line tension. POPC (1-palmitoyl-sn-2-oleoyl-glycero-3-phosphocholine), on the other hand, acts as a line-active hybrid lipid, reducing the domain size when added in small amounts and slowing down domain coarsening. Finally, we show that despite the regulation of domain size by both methods, the phase transition temperature is influenced by the presence of oil molecules but not significantly by the presence of hybrid lipids. Overall, our results show how to regulate domain size in binary membrane model systems, over a wide range of length scales, by incorporating oil molecules and hybrid lipids. American Chemical Society 2022-07-27 2022-08-11 /pmc/articles/PMC9377339/ /pubmed/35895895 http://dx.doi.org/10.1021/acs.jpcb.2c02862 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Scheidegger, Laura
Stricker, Laura
Beltramo, Peter J.
Vermant, Jan
Domain Size Regulation in Phospholipid Model Membranes Using Oil Molecules and Hybrid Lipids
title Domain Size Regulation in Phospholipid Model Membranes Using Oil Molecules and Hybrid Lipids
title_full Domain Size Regulation in Phospholipid Model Membranes Using Oil Molecules and Hybrid Lipids
title_fullStr Domain Size Regulation in Phospholipid Model Membranes Using Oil Molecules and Hybrid Lipids
title_full_unstemmed Domain Size Regulation in Phospholipid Model Membranes Using Oil Molecules and Hybrid Lipids
title_short Domain Size Regulation in Phospholipid Model Membranes Using Oil Molecules and Hybrid Lipids
title_sort domain size regulation in phospholipid model membranes using oil molecules and hybrid lipids
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9377339/
https://www.ncbi.nlm.nih.gov/pubmed/35895895
http://dx.doi.org/10.1021/acs.jpcb.2c02862
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