Heller W T, He K, Ludtke S J, Harroun T A, Huang H W
Physics Department, Rice University, Houston, Texas 77005-1892, USA.
Biophys J. 1997 Jul;73(1):239-44. doi: 10.1016/S0006-3495(97)78064-0.
Adsorption of amphiphilic peptides to the headgroup region of a lipid bilayer is a common mode of protein-membrane interactions. Previous studies have shown that adsorption causes membrane thinning. The degree of the thinning depends on the degree of the lateral expansion caused by the peptide adsorption. If this simple molecular mechanism is correct, the degree of lateral expansion and consequently the membrane thinning should depend on the size of the headgroup relative to the cross section of the hydrocarbon chains. Previously we have established the connection between the alamethicin insertion transition and the membrane thinning effect. In this paper we use oriented circular dichroism to study the effect of varying the size of the headgroup, while maintaining a constant cross section of the lipid chains, on the insertion transition. A simple quantitative prediction agrees very well with the experiment.
两亲性肽吸附到脂质双层的头部基团区域是蛋白质与膜相互作用的常见模式。先前的研究表明,吸附会导致膜变薄。变薄的程度取决于肽吸附引起的横向扩张程度。如果这个简单的分子机制是正确的,那么横向扩张的程度以及随之而来的膜变薄应该取决于头部基团相对于烃链横截面的大小。之前我们已经建立了短杆菌肽插入转变与膜变薄效应之间的联系。在本文中,我们使用取向圆二色性来研究在保持脂质链横截面不变的情况下,改变头部基团大小对插入转变的影响。一个简单的定量预测与实验结果非常吻合。