Chip electrophoretic characterization of liposomes with biological lipid composition: Coming closer to a model for viral infection

被引:14
作者
Bilek, Gerhard [1 ]
Weiss, Victor U. [1 ]
Pickl-Herk, Angela [1 ]
Blaas, Dieter [1 ]
Kenndler, Ernst [1 ]
机构
[1] Med Univ Vienna, Max F Perutz Labs, Inst Med Biochem, Ctr Mol Biol,VBC, A-1030 Vienna, Austria
基金
奥地利科学基金会;
关键词
Chip electrophoresis; 1,2-Dioleoyl-sn-glycero-3-[(N-(5-amino-1-carboxypentyl); iminodiacetic acid)succinyl] (nickel salt); Human Rhinovirus; Liposome; Receptor; VIRUS; SEPARATION; MEMBRANE; RECEPTOR;
D O I
10.1002/elps.200900382
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In first attempts at elucidating the transfer of the RNA genome of a human Rhinovirus through lipid membranes in vitro we made use of liposomes decorated with recombinant receptors. This model system was characterized previously by CE but suffered from the requirement for inclusion of polyethylene glycol-modified lipids for reliable separations [Weiss, V. U., Bilek, G., Pickl-Herk, A., Blaas, D., Kenndler, E., Electrophoresis 2009, 30, 2123-2128.]. We here report the analysis of liposomes with a lipid composition much more similar to that of biological lipid bilayers. We found that vesicles containing and lacking this non-physiologic lipid differ significantly in their electrophoretic mobility (by factor 2) although the concentration of charge-bearing lipids in their bilayers is the same. We demonstrate that binding of a human Rhinovirus to the latter liposomes decorated with a cognate receptor can be analysed via electrophoresis on microchips; we support our results with transmission electron microscopy.
引用
收藏
页码:4292 / 4299
页数:8
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