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Dependence of Micelle Size and Shape on Detergent Alkyl Chain Length and Head Group

Micelle-forming detergents provide an amphipathic environment that can mimic lipid bilayers and are important tools for solubilizing membrane proteins for functional and structural investigations in vitro. However, the formation of a soluble protein-detergent complex (PDC) currently relies on empiri...

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Autores principales: Oliver, Ryan C., Lipfert, Jan, Fox, Daniel A., Lo, Ryan H., Doniach, Sebastian, Columbus, Linda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648574/
https://www.ncbi.nlm.nih.gov/pubmed/23667481
http://dx.doi.org/10.1371/journal.pone.0062488
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author Oliver, Ryan C.
Lipfert, Jan
Fox, Daniel A.
Lo, Ryan H.
Doniach, Sebastian
Columbus, Linda
author_facet Oliver, Ryan C.
Lipfert, Jan
Fox, Daniel A.
Lo, Ryan H.
Doniach, Sebastian
Columbus, Linda
author_sort Oliver, Ryan C.
collection PubMed
description Micelle-forming detergents provide an amphipathic environment that can mimic lipid bilayers and are important tools for solubilizing membrane proteins for functional and structural investigations in vitro. However, the formation of a soluble protein-detergent complex (PDC) currently relies on empirical screening of detergents, and a stable and functional PDC is often not obtained. To provide a foundation for systematic comparisons between the properties of the detergent micelle and the resulting PDC, a comprehensive set of detergents commonly used for membrane protein studies are systematically investigated. Using small-angle X-ray scattering (SAXS), micelle shapes and sizes are determined for phosphocholines with 10, 12, and 14 alkyl carbons, glucosides with 8, 9, and 10 alkyl carbons, maltosides with 8, 10, and 12 alkyl carbons, and lysophosphatidyl glycerols with 14 and 16 alkyl carbons. The SAXS profiles are well described by two-component ellipsoid models, with an electron rich outer shell corresponding to the detergent head groups and a less electron dense hydrophobic core composed of the alkyl chains. The minor axis of the elliptical micelle core from these models is constrained by the length of the alkyl chain, and increases by 1.2–1.5 Å per carbon addition to the alkyl chain. The major elliptical axis also increases with chain length; however, the ellipticity remains approximately constant for each detergent series. In addition, the aggregation number of these detergents increases by ∼16 monomers per micelle for each alkyl carbon added. The data provide a comprehensive view of the determinants of micelle shape and size and provide a baseline for correlating micelle properties with protein-detergent interactions.
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spelling pubmed-36485742013-05-10 Dependence of Micelle Size and Shape on Detergent Alkyl Chain Length and Head Group Oliver, Ryan C. Lipfert, Jan Fox, Daniel A. Lo, Ryan H. Doniach, Sebastian Columbus, Linda PLoS One Research Article Micelle-forming detergents provide an amphipathic environment that can mimic lipid bilayers and are important tools for solubilizing membrane proteins for functional and structural investigations in vitro. However, the formation of a soluble protein-detergent complex (PDC) currently relies on empirical screening of detergents, and a stable and functional PDC is often not obtained. To provide a foundation for systematic comparisons between the properties of the detergent micelle and the resulting PDC, a comprehensive set of detergents commonly used for membrane protein studies are systematically investigated. Using small-angle X-ray scattering (SAXS), micelle shapes and sizes are determined for phosphocholines with 10, 12, and 14 alkyl carbons, glucosides with 8, 9, and 10 alkyl carbons, maltosides with 8, 10, and 12 alkyl carbons, and lysophosphatidyl glycerols with 14 and 16 alkyl carbons. The SAXS profiles are well described by two-component ellipsoid models, with an electron rich outer shell corresponding to the detergent head groups and a less electron dense hydrophobic core composed of the alkyl chains. The minor axis of the elliptical micelle core from these models is constrained by the length of the alkyl chain, and increases by 1.2–1.5 Å per carbon addition to the alkyl chain. The major elliptical axis also increases with chain length; however, the ellipticity remains approximately constant for each detergent series. In addition, the aggregation number of these detergents increases by ∼16 monomers per micelle for each alkyl carbon added. The data provide a comprehensive view of the determinants of micelle shape and size and provide a baseline for correlating micelle properties with protein-detergent interactions. Public Library of Science 2013-05-08 /pmc/articles/PMC3648574/ /pubmed/23667481 http://dx.doi.org/10.1371/journal.pone.0062488 Text en © 2013 Oliver et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Oliver, Ryan C.
Lipfert, Jan
Fox, Daniel A.
Lo, Ryan H.
Doniach, Sebastian
Columbus, Linda
Dependence of Micelle Size and Shape on Detergent Alkyl Chain Length and Head Group
title Dependence of Micelle Size and Shape on Detergent Alkyl Chain Length and Head Group
title_full Dependence of Micelle Size and Shape on Detergent Alkyl Chain Length and Head Group
title_fullStr Dependence of Micelle Size and Shape on Detergent Alkyl Chain Length and Head Group
title_full_unstemmed Dependence of Micelle Size and Shape on Detergent Alkyl Chain Length and Head Group
title_short Dependence of Micelle Size and Shape on Detergent Alkyl Chain Length and Head Group
title_sort dependence of micelle size and shape on detergent alkyl chain length and head group
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648574/
https://www.ncbi.nlm.nih.gov/pubmed/23667481
http://dx.doi.org/10.1371/journal.pone.0062488
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