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对含有较长链同系物的饱和磷脂酰胆碱的温度和压力诱导双层相变进行全面表征。

Comprehensive characterization of temperature- and pressure-induced bilayer phase transitions for saturated phosphatidylcholines containing longer chain homologs.

作者信息

Goto Masaki, Endo Takuya, Yano Takahiro, Tamai Nobutake, Kohlbrecher Joachim, Matsuki Hitoshi

机构信息

Laboratory for Neutron Scattering and Imaging, Paul Scherrer Institute, CH-5232 Villigen PSI, Switzerland.

Department of Biological Science and Technology, Faculty of Engineering, The University of Tokushima, 2-1 Minamijosanjima-cho, Tokushima 770-8506, Japan.

出版信息

Colloids Surf B Biointerfaces. 2015 Apr 1;128:389-397. doi: 10.1016/j.colsurfb.2015.02.036. Epub 2015 Feb 25.

Abstract

Complete elucidation of the phase behavior of phospholipid bilayers requires information on the subtransition from the lamellar crystal (Lc) phase to the gel phase. However, for bilayers of saturated diacylphosphatidylcholines (CnPCs), especially longer chain homologs, equilibration in the Lc phase is known to be very slow. In this study, bilayer phase transitions of three CnPCs with longer acyl chains, C19PC, C20PC and C21PC, were observed by differential scanning calorimetry under atmospheric pressure and by light-transmittance measurements under high pressure. Using lipid samples treated by thermal annealing enabled the observation of the sub-, pre- and main transitions of the C19PC and C20PC bilayers under atmospheric pressure. Only the pre- and main transitions could be observed for the C21PC bilayer due to very slow kinetics of the Lc phase formation for lipids with long acyl chains. The temperature and pressure phase diagrams constructed and phase-transitions quantities (enthalpy, entropy and volume changes) evaluated for these bilayers were compared with one another and with those of bilayers of the CnPC homologs examined in previous studies. These results allowed us (1) to clarify the temperature- and pressure-dependent phase sequence and phase stability of the CnPC (n=12-22) bilayers as a function of the hydrophobicity of the molecules, (2) to prove the presence of a shorter and a longer limit (n=13 and 21) in the acyl chain length for the pressure-induced bilayer interdigitation and (3) to reveal the chain-length dependence of the thermodynamic quantities of the subtransitions including the volume change.

摘要

要全面阐明磷脂双层的相行为,需要有关从层状晶体(Lc)相到凝胶相的亚转变的信息。然而,对于饱和二酰基磷脂酰胆碱(CnPCs)双层,尤其是长链同系物,已知在Lc相中的平衡非常缓慢。在本研究中,通过常压下的差示扫描量热法和高压下的透光率测量,观察了三种具有较长酰基链的CnPCs(C19PC、C20PC和C21PC)的双层相变。使用经过热退火处理的脂质样品,能够在常压下观察到C19PC和C20PC双层的亚转变、预转变和主转变。由于长酰基链脂质的Lc相形成动力学非常缓慢,对于C21PC双层只能观察到预转变和主转变。构建了这些双层的温度和压力相图,并评估了相变量(焓、熵和体积变化),将它们相互比较,并与先前研究中考察的CnPC同系物双层的相图和相变量进行比较。这些结果使我们能够:(1)阐明CnPC(n = 12 - 22)双层的温度和压力依赖性相序列和相稳定性与分子疏水性的关系;(2)证明在压力诱导的双层交叉指化中,酰基链长度存在较短和较长的极限(n = 13和21);(3)揭示包括体积变化在内的亚转变热力学量的链长依赖性。

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