STM Studies of Fusion of Cholesterol Suspensions and Mixed 1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC)/Cholesterol Vesicles onto a Au(111) Electrode Surface

Electrochemical scanning tunneling microscopy (EC-STM) has been applied to study the structure of the film formed by fusion of cholesterol suspensions and mixed dimyristoylphosphatidylcholine (DMPC)/cholesterol vesicles on a Au(111) electrode surface. It has been demonstrated that cholesterol molecu...

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Veröffentlicht in:Journal of the American Chemical Society 2008-04, Vol.130 (17), p.5736-5743
Hauptverfasser: Sek, Slawomir, Xu, Shimin, Chen, Maohui, Szymanski, Grzegorz, Lipkowski, Jacek
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Sprache:eng
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Zusammenfassung:Electrochemical scanning tunneling microscopy (EC-STM) has been applied to study the structure of the film formed by fusion of cholesterol suspensions and mixed dimyristoylphosphatidylcholine (DMPC)/cholesterol vesicles on a Au(111) electrode surface. It has been demonstrated that cholesterol molecules assemble at the gold support into several structures templated by the crystallography of the metal surface and involving flat or edge-on adsorbed molecules. Studies of the film formed by fusion of mixed DMPC/cholesterol vesicles revealed that ordered domains of either pure DMPC or pure cholesterol were formed. These results indicate that, at the metal surface, the molecules released by the rupture of a vesicle initially self-assemble into a well-ordered monolayer. The self-assembly is controlled by the hydrocarbon skeleton−metal surface interaction. In the case of mixed DMPC/cholesterol vesicles, the molecule−metal interactions induce segregation of the two components into single component domains. However, the molecule−metal interaction induced monolayer is a transient phenomenon. When more molecules accumulate at the surface, the molecule−molecule interactions dominate the assembly, and the monolayer is transformed into a bilayer.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja711020q