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Lipid Concentration and Molar Ratio Boundaries for the Use of Isotropic Bicelles

[Image: see text] Bicelles are model membranes generally made of long-chain dimyristoylphosphatidylcholine (DMPC) and short-chain dihexanoyl-PC (DHPC). They are extensively used in the study of membrane interactions and structure determination of membrane-associated peptides, since their composition...

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Autores principales: Beaugrand, Maïwenn, Arnold, Alexandre A., Hénin, Jérôme, Warschawski, Dror E., Williamson, Philip T. F., Marcotte, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072726/
https://www.ncbi.nlm.nih.gov/pubmed/24797658
http://dx.doi.org/10.1021/la5004353
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author Beaugrand, Maïwenn
Arnold, Alexandre A.
Hénin, Jérôme
Warschawski, Dror E.
Williamson, Philip T. F.
Marcotte, Isabelle
author_facet Beaugrand, Maïwenn
Arnold, Alexandre A.
Hénin, Jérôme
Warschawski, Dror E.
Williamson, Philip T. F.
Marcotte, Isabelle
author_sort Beaugrand, Maïwenn
collection PubMed
description [Image: see text] Bicelles are model membranes generally made of long-chain dimyristoylphosphatidylcholine (DMPC) and short-chain dihexanoyl-PC (DHPC). They are extensively used in the study of membrane interactions and structure determination of membrane-associated peptides, since their composition and morphology mimic the widespread PC-rich natural eukaryotic membranes. At low DMPC/DHPC (q) molar ratios, fast-tumbling bicelles are formed in which the DMPC bilayer is stabilized by DHPC molecules in the high-curvature rim region. Experimental constraints imposed by techniques such as circular dichroism, dynamic light scattering, or microscopy may require the use of bicelles at high dilutions. Studies have shown that such conditions induce the formation of small aggregates and alter the lipid-to-detergent ratio of the bicelle assemblies. The objectives of this work were to determine the exact composition of those DMPC/DHPC isotropic bicelles and study the lipid miscibility. This was done using (31)P nuclear magnetic resonance (NMR) and exploring a wide range of lipid concentrations (2–400 mM) and q ratios (0.15–2). Our data demonstrate how dilution modifies the actual DMPC/DHPC molar ratio in the bicelles. Care must be taken for samples with a total lipid concentration ≤250 mM and especially at q ∼ 1.5–2, since moderate dilutions could lead to the formation of large and slow-tumbling lipid structures that could hinder the use of solution NMR methods, circular dichroism or dynamic light scattering studies. Our results, supported by infrared spectroscopy and molecular dynamics simulations, also show that phospholipids in bicelles are largely segregated only when q > 1. Boundaries are presented within which control of the bicelles’ q ratio is possible. This work, thus, intends to guide the choice of q ratio and total phospholipid concentration when using isotropic bicelles.
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spelling pubmed-40727262014-06-27 Lipid Concentration and Molar Ratio Boundaries for the Use of Isotropic Bicelles Beaugrand, Maïwenn Arnold, Alexandre A. Hénin, Jérôme Warschawski, Dror E. Williamson, Philip T. F. Marcotte, Isabelle Langmuir [Image: see text] Bicelles are model membranes generally made of long-chain dimyristoylphosphatidylcholine (DMPC) and short-chain dihexanoyl-PC (DHPC). They are extensively used in the study of membrane interactions and structure determination of membrane-associated peptides, since their composition and morphology mimic the widespread PC-rich natural eukaryotic membranes. At low DMPC/DHPC (q) molar ratios, fast-tumbling bicelles are formed in which the DMPC bilayer is stabilized by DHPC molecules in the high-curvature rim region. Experimental constraints imposed by techniques such as circular dichroism, dynamic light scattering, or microscopy may require the use of bicelles at high dilutions. Studies have shown that such conditions induce the formation of small aggregates and alter the lipid-to-detergent ratio of the bicelle assemblies. The objectives of this work were to determine the exact composition of those DMPC/DHPC isotropic bicelles and study the lipid miscibility. This was done using (31)P nuclear magnetic resonance (NMR) and exploring a wide range of lipid concentrations (2–400 mM) and q ratios (0.15–2). Our data demonstrate how dilution modifies the actual DMPC/DHPC molar ratio in the bicelles. Care must be taken for samples with a total lipid concentration ≤250 mM and especially at q ∼ 1.5–2, since moderate dilutions could lead to the formation of large and slow-tumbling lipid structures that could hinder the use of solution NMR methods, circular dichroism or dynamic light scattering studies. Our results, supported by infrared spectroscopy and molecular dynamics simulations, also show that phospholipids in bicelles are largely segregated only when q > 1. Boundaries are presented within which control of the bicelles’ q ratio is possible. This work, thus, intends to guide the choice of q ratio and total phospholipid concentration when using isotropic bicelles. American Chemical Society 2014-05-05 2014-06-03 /pmc/articles/PMC4072726/ /pubmed/24797658 http://dx.doi.org/10.1021/la5004353 Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Beaugrand, Maïwenn
Arnold, Alexandre A.
Hénin, Jérôme
Warschawski, Dror E.
Williamson, Philip T. F.
Marcotte, Isabelle
Lipid Concentration and Molar Ratio Boundaries for the Use of Isotropic Bicelles
title Lipid Concentration and Molar Ratio Boundaries for the Use of Isotropic Bicelles
title_full Lipid Concentration and Molar Ratio Boundaries for the Use of Isotropic Bicelles
title_fullStr Lipid Concentration and Molar Ratio Boundaries for the Use of Isotropic Bicelles
title_full_unstemmed Lipid Concentration and Molar Ratio Boundaries for the Use of Isotropic Bicelles
title_short Lipid Concentration and Molar Ratio Boundaries for the Use of Isotropic Bicelles
title_sort lipid concentration and molar ratio boundaries for the use of isotropic bicelles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072726/
https://www.ncbi.nlm.nih.gov/pubmed/24797658
http://dx.doi.org/10.1021/la5004353
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