Rupture Pathway of Phosphatidylcholine Liposomes on Silicon Dioxide

被引:52
作者
Reimhult, Erik [1 ,2 ]
Kasemo, Bengt [1 ]
Hook, Fredrik [1 ]
机构
[1] Chalmers, Dept Appl Phys, SE-41296 Gothenburg, Sweden
[2] Swiss Fed Inst Technol Zurich ETH Zurich, Dept Mat, Surface Sci & Technol Lab, CH-8093 Zurich, Switzerland
来源
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | 2009年 / 10卷 / 04期
基金
瑞士国家科学基金会; 瑞典研究理事会;
关键词
Lipid Vesicle; Supported Bilayer; Quartz Crystal Microbalance with Dissipation Monitoring (QCM-D); Adsorption; Asymmetric Labeling; SUPPORTED PHOSPHOLIPID-BILAYERS; QUARTZ-CRYSTAL MICROBALANCE; ATOMIC-FORCE MICROSCOPY; LIPID-BILAYERS; VESICLE ADSORPTION; PROTEIN ADSORPTION; IN-SITU; QCM-D; MEMBRANES; AFM;
D O I
10.3390/ijms10041683
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have investigated the pathway by which unilamellar POPC liposomes upon adsorption undergo rupture and form a supported lipid bilayer (SLB) on a SiO2 surface. Biotinylated lipids were selectively incorporated in the outer monolayer of POPC liposomes to create liposomes with asymmetric lipid compositions in the outer and inner leaflets. The specific binding of neutravidin and anti-biotin to SLBs formed by liposome fusion, prior to and after equilibrated flip-flop between the upper and lower monolayers in the SLB, were then investigated. It was concluded that the lipids in the outer monolayer of the vesicle predominantly end up on the SLB side facing the SiO2 substrate, as demonstrated by having maximum 30-40% of lipids in the liposome outer monolayer orienting towards the bulk after forming the SLB.
引用
收藏
页码:1683 / 1696
页数:14
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