Division of Chemical Engineering, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka, Japan.
Colloids Surf B Biointerfaces. 2011 Nov 1;88(1):221-30. doi: 10.1016/j.colsurfb.2011.06.036. Epub 2011 Jul 20.
In this study, we investigated the dynamics of a membrane interface of liposomes prepared by eight zwitterionic phosphatidylcholines in terms of their headgroup mobility, with spectroscopic methods such as dielectric dispersion analysis (DDA), fluorescence spectroscopy. The DDA measurement is based on the response of the permanent dipole moment to a driving electric field and could give the information on the axial rotational Brownian motion of a headgroup with the permanent dipole moment. This motion depended on kinds of phospholipids, the diameter of the liposomes, and the temperature. The activation energy required to overcome the intermolecular force between headgroups of phospholipids depended on the strength of the interaction between headgroups such as hydrogen bonds and/or dipole-dipole interaction. Hydration at the phosphorous group of phospholipid and the molecular order of lipid membrane impaired the interaction between headgroups. Furthermore, the hydrophobicity of membrane surface increased parallel to the increase in headgroup mobility. It is, therefore, concluded that hydration of headgroup promoted its mobility to make the membrane surface hydrophobic. The lipid membrane in liquid crystalline phase or the lipid membrane with the larger curvature was more hydrophobic.
在这项研究中,我们通过介电色散分析(DDA)、荧光光谱等光谱方法,研究了由八种两性离子磷脂制备的脂质体膜界面的动力学,以研究其头部基团的迁移率。DDA 测量基于永久偶极矩对驱动电场的响应,可提供具有永久偶极矩的头部基团轴向旋转布朗运动的信息。这种运动取决于磷脂的种类、脂质体的直径和温度。克服磷脂头部基团之间分子间力所需的活化能取决于头部基团之间的相互作用强度,如氢键和/或偶极-偶极相互作用。在磷脂的磷基团处的水合作用和脂质膜的分子有序性会损害头部基团之间的相互作用。此外,膜表面的疏水性与头部基团迁移率的增加平行增加。因此,可以得出结论,头部基团的水合作用促进了其迁移率,从而使膜表面疏水。液晶相中的脂质膜或曲率较大的脂质膜具有更高的疏水性。