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231225s2017 xx |||||o 00| ||eng c |
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|a 10.1021/acs.langmuir.7b03742
|2 doi
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|a pubmed24n0927.xml
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|a (DE-627)NLM278262422
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|a (NLM)29160078
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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 Oluwole, Abraham Olusegun
|e verfasserin
|4 aut
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|a Formation of Lipid-Bilayer Nanodiscs by Diisobutylene/Maleic Acid (DIBMA) Copolymer
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|c 2017
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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 18.01.2019
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|a Date Revised 18.01.2019
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Membrane proteins usually need to be extracted from their native environment and separated from other membrane components for in-depth in vitro characterization. The use of styrene/maleic acid (SMA) copolymers to solubilize membrane proteins and their surrounding lipids into bilayer nanodiscs is an attractive approach toward this goal. We have recently shown that a diisobutylene/maleic acid (DIBMA) copolymer similarly solubilizes model and cellular membranes but, unlike SMA(3:1), has a mild impact on lipid acyl-chain order and thermotropic phase behavior. Here, we used fluorescence spectroscopy, small-angle X-ray scattering, size-exclusion chromatography, dynamic light scattering, and 31P nuclear magnetic resonance spectroscopy to examine the self-association of DIBMA and its membrane-solubilization properties against lipids differing in acyl-chain length and saturation. Although DIBMA is less hydrophobic than commonly used SMA(3:1) and SMA(2:1) copolymers, it efficiently formed lipid-bilayer nanodiscs that decreased in size with increasing polymer/lipid ratio while maintaining the overall thickness of the membrane. DIBMA fractions of different molar masses were similarly efficient in solubilizing a saturated lipid. Coulomb screening at elevated ionic strength or reduced charge density on the polymer at low pH enhanced the solubilization efficiency of DIBMA. The free-energy penalty for transferring phospholipids from vesicular bilayers into nanodiscs became more unfavorable with increasing acyl-chain length and unsaturation. Altogether, these findings provide a rational framework for using DIBMA in membrane-protein research by shedding light on the effects of polymer and lipid properties as well as experimental conditions on membrane solubilization
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Alkenes
|2 NLM
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|a Lipid Bilayers
|2 NLM
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|a Maleates
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|a maleic acid
|2 NLM
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|a 91XW058U2C
|2 NLM
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|a diisobutylene
|2 NLM
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|a N69L73ADVF
|2 NLM
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|a Klingler, Johannes
|e verfasserin
|4 aut
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|a Danielczak, Bartholomäus
|e verfasserin
|4 aut
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|a Babalola, Jonathan Oyebamiji
|e verfasserin
|4 aut
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|a Vargas, Carolyn
|e verfasserin
|4 aut
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|a Pabst, Georg
|e verfasserin
|4 aut
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|a Keller, Sandro
|e verfasserin
|4 aut
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 33(2017), 50 vom: 19. Dez., Seite 14378-14388
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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|g volume:33
|g year:2017
|g number:50
|g day:19
|g month:12
|g pages:14378-14388
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|u http://dx.doi.org/10.1021/acs.langmuir.7b03742
|3 Volltext
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|a AR
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|d 33
|j 2017
|e 50
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|c 12
|h 14378-14388
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