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Thermally induced phase separation in supported bilayers of glycosphingolipid and phospholipid mixtures

机译:热诱导相分离的糖鞘脂和磷脂混合物的双层支撑

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The authors have studied microstructure evolution during thermally induced phase separation in a class of binary supported lipid bilayers using a quantitative application of imaging ellipsometry. The bilayers consist of binary mixtures consisting of a higher melting glycosphingolipid, galactosylceramide (GalCer), which resides primarily in the outer leaflet, and a lower melting, unsaturated phospholipid, 1,2-dilauroyl-sn-glycero-3-phosphocholine (DLPC). Three different bilayer compositions of GalCer/DLPC mixtures at 35:65, 20:80, and 10:90 molar ratios were cooled at controlled rates from their high-temperature homogeneous phase to temperatures corresponding to their phase coexistence regime and imaged in real time using imaging ellipsometry. During the thermotropic course of GalCer gelation, we find that two distinct types of morphological features modulate. First, the formation and growth of chain and fractal-like defects ascribed to the net change in molecular areas during the phase transition. The formation of these defects is consistent with the expected contraction in the molecular area during the liquid crystalline to gel-phase transition. Second, the nucleation and growth of irregularly shaped gel-phase domains, which exhibit either line-tension dominated compact shape or dendritic domains with extended interfaces. Quantifying domain morphology within the fractal framework reveals a close correspondence, and the quantization of the transition width confirms previous estimates of reduced phase transition cooperativity in supported bilayers. A comparison of domain properties indicates that thermal history, bilayer composition, and cooling rate all influence microstructure details including shapes, sizes, and distributions of domains and defects: At lower cooling rates and lower GalCer fractions compact domains form and at higher GalCer fractions (or at higher cooling rates) dendritic domains are evident. This transition of domain morphology from compact shapes to dendritic shapes at higher cooling rates and higher relative fractions of GalCer suggests kinetic control of shape equilibration in these phospho- and glycolipid mixtures.
机译:作者使用成像椭偏仪的定量应用研究了一类二元支撑脂质双层在热诱导相分离过程中的微观结构演变。双层膜由二元混合物组成,该混合物由较高熔点的糖鞘脂,半乳糖神经酰胺(GalCer)(主要位于外部小叶中)和较低熔点的不饱和磷脂,1,2-二聚十二烷基-sn-甘油-3-磷酸胆碱(DLPC)组成。将三种不同的摩尔比分别为35:65、20:80和10:90的GalCer / DLPC混合物的双层成分从其高温均相冷却到与其相共存状态相对应的温度,并使用椭圆偏振成像。在GalCer凝胶的热致过程中,我们发现两种不同类型的形态特征发生了调节。首先,链和分形缺陷的形成和增长归因于相变过程中分子区域的净变化。这些缺陷的形成与液晶向凝胶相转变期间分子区域中预期的收缩相一致。第二,不规则形状的凝胶相域的成核和生长,其表现出线张力为主的紧凑形状或具有扩展界面的树枝状域。量化分形框架内的畴形态揭示了紧密的对应关系,并且过渡宽度的量化确认了先前对支持的双层中相变合作性降低的估计。磁畴特性的比较表明,热历史,双层成分和冷却速率都会影响微观结构的细节,包括磁畴和缺陷的形状,大小和分布:在较低的冷却速率和较低的GalCer分数下,会形成致密磁畴,而在较高的GalCer分数下(或在较高的冷却速率下)树枝状区域是明显的。在较高的冷却速率和较高的GalCer相对分数下,畴形态从致密形状转变为树状形状,表明在这些磷脂和糖脂混合物中,动力学控制了形状平衡。

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