Hepatitis A synthetic peptide VP3(110-121) miscibility with dipalmitoylphosphatidylcholine, dipalmitoylphosphatidylglycerol, and stearylamine monolayers

被引:4
|
作者
Sospedra, P
Alsina, MA
Espina, M
Reig, F
Haro, I
Mestres, C
机构
[1] Fac Farm, Dept Phys Chem, Barcelona 08028, Spain
[2] CSIC, IIQAB, Dept Peptide & Prot Chem, Barcelona 08034, Spain
关键词
hepatitis A; synthetic vaccine; lipid monolayers; lipid-peptide interaction;
D O I
10.1006/jcis.1999.6585
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
To prepare liposomes containing a synthetic hepatitis A virus antigen (HAV) [VP3(110-121)] as a vaccine, the miscibility of this peptide (with negative net charge) with a neutral lipid [dipalmitoylphosphatidylcholine (DPPC)], a negatively charged lipid [dipalmitoylphosphatidylglycerol (DPPG)], and a positively charged lipid [Stearylamine (SA)] was studied through compression isotherms of monolayers. Mixtures with DPPC and SA showed a low degree of interaction with the peptide, the composition of the monolayer being stable through compression. For DPPG-containing monolayers larger positive deviations from ideality were found, and the peptide was squeezed out from the monolayer at a DPPG/VP3(110-121) mole fraction of 0.8/0.2. All this suggests that besides hydrophobic interactions between the peptide and the lipid, electrostatic forces also play a role; thus it seems that neutral and positively charged lipids would be more suitable for preparing stable liposomes with VP3(110-121). (C) 2000 Academic Press.
引用
收藏
页码:230 / 235
页数:6
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