Physisorbed Polymer-Tethered Lipid Bilayer with Lipopolymer Gradient

被引:10
|
作者
Lin, Yu-Hung [1 ]
Minner, Daniel E. [1 ,2 ]
Herring, Vincent L. [1 ]
Naumann, Christoph A. [1 ]
机构
[1] Indiana Univ Purdue Univ, Dept Chem & Chem Biol, Indianapolis, IN 46202 USA
[2] Indiana Univ Purdue Univ, Integrated Nanosyst Dev Inst, Indianapolis, IN 46202 USA
来源
MATERIALS | 2012年 / 5卷 / 11期
基金
美国国家科学基金会;
关键词
gradient bilayer; Langmuir-Blodgett transfer; lipopolymer; polymer-tethered lipid membrane; Epifluorescence; atomic force microscopy; buckling structure; SUPPORTED PHOSPHOLIPID-BILAYERS; MEMBRANE-PROTEINS; CELL RECEPTORS; ADHESION; MIXTURES; SUBSTRATE; SURFACE; ENERGY; FILMS;
D O I
10.3390/ma5112243
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Physisorbed polymer-tethered lipid bilayers consisting of phospholipids and lipopolymers represent an attractive planar model membrane platform, in which bilayer fluidity and membrane elastic properties can be regulated through lipopolymer molar concentration. Herein we report a method for the fabrication of such a planar model membrane system with a lateral gradient of lipopolymer density. In addition, a procedure is described, which leads to a sharp boundary between regions of low and high lipopolymer molar concentrations. Resulting gradients and sharp boundaries are visualized on the basis of membrane buckling structures at elevated lipopolymer concentrations using epifluorescence microscopy and atomic force microscopy. Furthermore, results from spot photobleaching experiments are presented, which provide insight into the lipid lateral fluidity in these model membrane architectures. The presented experimental data highlight a planar, solid-supported membrane characterized by fascinating length scale-dependent dynamics and elastic properties with remarkable parallels to those observed in cellular membranes.
引用
收藏
页码:2243 / 2257
页数:15
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