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231224s2013 xx |||||o 00| ||eng c |
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|a 10.1021/la3024698
|2 doi
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|a pubmed24n0749.xml
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|a (DE-627)NLM224680544
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|a (NLM)23373466
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Wadsäter, Maria
|e verfasserin
|4 aut
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|a Effect of phospholipid composition and phase on nanodisc films at the solid-liquid interface as studied by neutron reflectivity
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|c 2013
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 16.08.2013
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|a Date Revised 21.11.2013
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Nanodiscs are disc-like self-assembled structures formed by phospholipids and amphipatic proteins. The proteins wrap like a belt around the hydrophobic part of the lipids, basically producing nanometer-sized patches of lipid bilayers. The bilayer in the nanodisc constitutes a native-like model of the cell membrane and can act as a nanometer-sized container for functional single membrane proteins. In this study, we present a general nanodisc-based system, intended for structural and functional studies of membrane proteins. In this method, the nanodiscs are aligned at a solid surface, providing the ability to determine the average structure of the film along an axis perpendicular to the interface as measured by neutron reflectivity. The nanodisc film was optimized in terms of nanodisc coverage, reduced film roughness, and stability for time-consuming studies. This was achieved by a systematic variation of the lipid phase, charge, and length of lipid tails. Herein, we show that, although all studied nanodiscs align with their lipid bilayer parallel to the interface, gel-phase DMPC nanodiscs form the most suitable film for future membrane protein studies since they yield a dense irreversibly adsorbed film with low roughness and high stability over time. This may be explained by the appropriate matching between the thickness of the hydrophobic lipid core of gel phase DMPC and the height of the belt protein. Moreover, once formed the gel-phase DMPC nanodiscs film can be heated up to melt the lipid bilayer, thus providing a more biologically friendly environment for membrane proteins
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Gels
|2 NLM
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|a Lipid Bilayers
|2 NLM
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|a Membrane Proteins
|2 NLM
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|a Phospholipids
|2 NLM
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|a Deuterium
|2 NLM
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|a AR09D82C7G
|2 NLM
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|a Barker, Robert
|e verfasserin
|4 aut
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|a Mortensen, Kell
|e verfasserin
|4 aut
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|a Feidenhans'l, Robert
|e verfasserin
|4 aut
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|a Cárdenas, Marité
|e verfasserin
|4 aut
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 29(2013), 9 vom: 05. März, Seite 2871-80
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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|g volume:29
|g year:2013
|g number:9
|g day:05
|g month:03
|g pages:2871-80
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|u http://dx.doi.org/10.1021/la3024698
|3 Volltext
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