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通过压力微扰量热法和密度法对酯键和醚键连接的脂质双层的体积特性进行表征。

Volumetric characterization of ester- and ether-linked lipid bilayers by pressure perturbation calorimetry and densitometry.

机构信息

Department of Life System, Institute of Technology and Science, The University of Tokushima, Tokushima, Japan.

出版信息

Colloids Surf B Biointerfaces. 2012 Apr 1;92:232-9. doi: 10.1016/j.colsurfb.2011.11.055. Epub 2011 Dec 21.

Abstract

We investigated the thermotropic volume behavior of dimyristoylphosphatidylcholine (DMPC), dipalmitoylphosphatidylcholine (DPPC) and dihexadecylphosphatidylcholine (DHPC) membranes using pressure perturbation calorimetry (PPC) and densitometry. The ln φ(2) vs temperature curves (φ(2): apparent molar volume of phospholipid) obtained from the PPC data using an analysis method that we developed agreed with the results from the density measurements for these lipids within the relative difference of about 0.62%. From those curves, the volume changes with the main transition were estimated at 18.0±0.49, 23.5±2.33 and 23.0±0.33 cm(3) mol(-1) for DMPC, DPPC and DHPC, respectively. For DPPC and DMPC, the average volume per methylene group of the hydrocarbon chains v(CH2) calculated by referring to the procedure by Nagle and Wilkinson was consistent with the previous result, which indicates that the DPPC bilayer in the gel state has denser hydrophobic bilayer core than the DMPC bilayer. For DHPC, the volume of the headgroup region v(H) was calculated to be 244 Å(3) by assuming that v(CH2) of DHPC equals that of DPPC above 45°C. This value was comparable to that of DPPC when the volume of the carbonyl groups was considered, which may signify that there is no significant conformational difference in the polar headgroups of both phospholipids. However, it was suggested from the consideration on v(H) of DHPC at 20°C that expansion of the headgroup region should occur as the interdigitated structure is formed, which means some conformational change of the headgroup region is induced by the interdigitation.

摘要

我们使用压力微扰量热法(PPC)和密度法研究了二肉豆蔻酰磷脂酰胆碱(DMPC)、二棕榈酰磷脂酰胆碱(DPPC)和二硬脂酰磷脂酰胆碱(DHPC)膜的热致体积行为。我们开发的分析方法从 PPC 数据得到的 ln φ(2) 与温度曲线(φ(2):磷脂的表观摩尔体积)与这些脂质的密度测量结果一致,相对差异约为 0.62%。从这些曲线中,我们估算了主相变时的体积变化,分别为 DMPC、DPPC 和 DHPC 的 18.0±0.49、23.5±2.33 和 23.0±0.33cm(3)mol(-1)。对于 DPPC 和 DMPC,通过参考 Nagle 和 Wilkinson 的程序计算的烃链每个亚甲基的平均体积 v(CH2)与以前的结果一致,这表明凝胶态的 DPPC 双层具有比 DMPC 双层更密集的疏水性双层核心。对于 DHPC,通过假设 DHPC 的 v(CH2)在 45°C 以上等于 DPPC 的 v(CH2),计算出头部区域 v(H)的体积为 244Å(3)。当考虑羰基的体积时,该值与 DPPC 的体积相当,这可能表明两种磷脂的极性头部基团没有明显的构象差异。然而,从 20°C 时 DHPC 的 v(H)的考虑表明,当形成互穿插结构时,头部区域应该会扩张,这意味着头部区域的构象变化是由互穿插引起的。

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