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Confocal Raman Microscopy Investigation of Phospholipid Monolayers Deposited on Nitrile-Modified Surfaces in Porous Silica Particles

机译:聚焦拉曼显微镜磷脂单层沉积在多孔二氧化硅颗粒中丁腈改性表面的磷脂单层

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Phospholipid bilayers deposited on a variety of surfaces provide models for investigation of the lipid membrane structure and supports for biocompatible sensors. Hybrid-supported phospholipid bilayers (HSLBs) are stable membrane models for these investigations, typically prepared by self-assembly of a lipid monolayer over an n-alkane-modified surface. HSLBs have been prepared on nalkyl chain-modified silica and used for lipophilicity-based chromatographic separations. The structure of these hybrid bilayers differs from vesicle membranes where the lipid head group spacing is greater due to interdigitation of the lipid acyl chains with the underlying n-alkyl chains bound to the silica surface. This interdigitated structure exhibits a broader melting transition at a higher temperature due to strong interactions between the lipid acyl chains and the immobile n-alkyl chains bound to silica. In the present work, we seek to reduce the interactions between a lipid monolayer and its supporting substrate by self-assembly of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) on porous silica functionalized with nitrile-terminated surface ligands. The frequency of Raman scattering of the surface -C N stretching mode at the lipid-nitrile interface is consistent with an n-alkane-like environment and insensitive to lipid head group charge, indicating that the lipid acyl chains are in contact with the surface nitrile groups. The head group area of this lipid monolayer was determined from the within-particle phospholipid concentration and silica specific surface area and found to be 54 +/- 2 A(2), equivalent to the head group area of a DMPC vesicle bilayer. The structure of these nitrile-supported phospholipid monolayers was characterized below and above their melting transition by confocal Raman microscopy and found to be nearly identical to DMPC vesicle bilayers. Their narrow gel-to-fluid-phase melting transition is equivalent to dispersed DMPC vesicles, suggesting that the acyl chain structure on the nitrile support mimics the outer leaflet structure of a vesicle membrane.
机译:沉积在各种表面磷脂双层的生物相容的传感器提供脂质膜结构体的调查模型和载体。混合支持磷脂双层(HSLBs)是用于这些研究稳定膜模型,典型地通过自组装的脂质单层的在n烷烃改性的表面上而制备。 HSLBs已经制备上n烷基链改性的二氧化硅和用于基于亲脂性色谱分离。从泡囊膜这些混合的不同的双层其中脂质头部基团的间隔较大,由于脂质酰基链与结合到二氧化硅表面的底层正烷基链交错的结构。此交叉指型结构显示由于结合到二氧化硅的脂质酰基链和不动的正烷基链之间的强相互作用在较高温度下更广泛的熔融转变。在目前的工作中,我们试图通过减少和它的支撑衬底上的脂质单层之间的相互作用自组装1,2-二肉豆蔻酰-sn-甘油-3-磷酸胆碱(DMPC)的与腈基封端的表面配体官能化多孔二氧化硅。在脂质腈界面的表面-CN拉伸模式的拉曼散射的频率是具有正烷烃类环境一致和不敏感的脂质头部基团的电荷,这表明脂质酰基链是与表面腈基接触。此脂质单层的头基面积从内颗粒磷脂浓度和二氧化硅的比表面积测定,结果为54 +/- 2 A(2),相当于的DMPC泡囊双分子头基面积。这些腈支持的磷脂单层的结构进行了表征下方和上方通过共焦拉曼显微镜其熔化转变,结果为几乎相同DMPC囊泡双分子层。其窄的凝胶 - 流体相熔化转变相当于分散DMPC囊泡,这表明在腈支持模拟物的囊泡膜的外小叶结构的酰基链结构。

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