Cholesteryl oligoethyleneglycol glycosides: Fluidizing effect of their embedment into phospholipid bilayers

被引:18
作者
Bardonnet, PL
Faivre, V
Pirot, F
Boullanger, P
Falson, F
机构
[1] Univ Lyon 1, Lab Pharm Galen Ind, ISPB, EA 3741, F-69373 Lyon, France
[2] Ctr Interuniv Pharmapeptides, F-74166 Archamps, France
[3] Univ Lyon 1, CNRS, UMR 5181, F-69622 Villeurbanne, France
关键词
glycolipid; liposome; phospholipid; cholesterol; differential scanning calorimetry; fluorescence; zeta potential; agglutination; lectin;
D O I
10.1016/j.bbrc.2005.02.092
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
Glycosides of cholesteryl oligoethyleneglycols have been synthesized and embedded in liposome bilayers. Several methods as steady-state fluorescence polarization, differential scanning calorimetry, zeta potential, and agglutination have been used to describe the physicochemical outcome of the incorporation of these synthetic glycolipids within phospholipid layers. From calorimetry and fluorescence experiments, it is apparent that the glycolipids decrease the transition temperature of the bilayers in a more important extent than cholesterol. Furthermore, the thickness of the aqueous layer fixed around the liposome is independent of the presence of glycolipids, suggesting that their hydrophilic parts (tetraethyleneglycol spacer and sugar moiety) are not completely extended towards the aqueous phase. Nevertheless, an important and specific interaction has been observed between such glycosylated liposomes and vegetal lectins. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1186 / 1192
页数:7
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