Fusion of small unilamellar vesicles onto laterally mixed self-assembled monolayers of thiolipopeptides

被引:34
作者
Baumgart, T
Kreiter, M
Lauer, H
Naumann, R
Jung, G
Jonczyk, A
Offenhäusser, A
Knoll, W
机构
[1] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[2] Univ Tubingen, D-72076 Tubingen, Germany
[3] Merck KGaA, D-64271 Darmstadt, Germany
关键词
solid-supported lipid bilayers; solid-supported lipid membranes; tethered membranes; thiolipopeptide; thiopeptide; surface plasmon resonance spectroscopy; impedance spectroscopy; fluorescence microscopy;
D O I
10.1016/S0021-9797(02)00098-X
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
Monolayers of the thiolipopeptide NH2-Cys-Ala-Ser-Ala-Ala-Ser-Ser-Ala-Pro-Ser-Ser-(Myr)Lys(Myr)-OH (III) were formed on gold surfaces by self-assembly, mixed with a lateral spacer of the same peptide composition, NH2-Cys-Ala-Ser-Ala-Ala-Ser-Ser-AlaPro-Ser-Ser-Lys-OH (I). Different mixing ratios were employed ranging from 0.1 to 1, corresponding to 10-100% thiolipopeptide. These self-assembled monolayers (SAMs) were then exposed to a suspension of liposomes with the aim of forming lipid bilayers as a function of the mixing ratio. A clear optimum with respect to homogeneity and electrical properties of the membranes was obtained in the middle region (0.5) of mixing ratio, as revealed by surface plasmon resonance spectroscopy, impedance spectroscopy, and fluorescence microscopy. The combination of these methods was shown to be a powerful tool, although a true lipid bilayer was not obtained. Instead, vesicle adsorption was shown to be the predominant process, and FRAP (fluorescence recovery after photobleaching) measurements showed that the films were not fluid on the micrometer length scale. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:298 / 309
页数:12
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