Effect of lipid headgroup composition on the interaction between melittin and lipid bilayers

被引:62
|
作者
Stromstedt, Adam A.
Wessman, Per
Ringstad, Lovisa
Edwards, Katarina
Malmsten, Martin
机构
[1] Uppsala Univ, Dept Pharm, SE-75123 Uppsala, Sweden
[2] Uppsala Univ, Dept Phys & Analyt Chem, SE-75123 Uppsala, Sweden
关键词
adsorption; bilayer; circular dichroism; ellipsometry; fluorescence; liposome; melittin;
D O I
10.1016/j.jcis.2007.02.070
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
The effect of the lipid polar headgroup on melittin-phospholipid interaction was investigated by cryo-TEM, fluorescence spectroscopy, ellipsometry, circular dichroism, electrophoresis and photon correlation spectroscopy. In particular, focus was placed on the effect of the lipid polar headgroup on peptide adsorption to, and penetration into, the lipid bilayer, as well as on resulting colloidal stability effects for large unilamellar liposomes. The effect of phospholipid headgroup properties on melittin-bilayer interaction was addressed by comparing liposomes containing phosphatidylcholine, -acid, and -inositol at varying ionic strength. Increasing the bilayer negative charge leads to an increased liposome tolerance toward melittin which is due to an electrostatic arrest of melittin at the membrane interface. Balancing the electrostatic attraction between the melittin positive charges and the phospholipid negative charges through a hydration repulsion, caused by inositol, reduced this surface arrest and increased liposome susceptibility to the disruptive actions of melittin. Furthermore, melittin was demonstrated to induce liposome structural destabilization on a colloidal scale which coincided with leakage induction for both anionic and zwitterionic systems. The latter findings thus clearly show that coalescence, aggregation, and fragmentation contribute to melittin-induced liposome leakage, and that detailed molecular analyses of melittin pore formation are incomplete without considering also these colloidal aspects. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:59 / 69
页数:11
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