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Micropatterned Fluid Lipid Bilayer Arrays Created Using a Continuous Flow Microspotter

机译:使用连续流动微量点样仪创建的微图案化流体脂质双层阵列

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We have developed a new method for creating micropatterned lipid bilayer arrays (MLBAs) using a 3D microfluidic system. An array of fluid lipid membranes was patterned onto a glass substrate using a Continuous Flow Microspotter. Fluorescence microscopy experiments were used to verify the formation of a bilayer structure on the glass substrate. Fluorescence recovery after photobleaching experiments demonstrated the bilayers' fluidity was maintained while being individually corralled on the substrate. The reproducibility of bilayer formation within an array was demonstrated by the linear response of membrane fluorescence versus mol percent rhodamine functionalized lipids incorporated into the vesicles prior to fusion to the surface. The highly customizable nature of the MLBAs was demonstrated utilizing three different fluorescently labeled lipids to generate a multiple component lipid array. Finally, the cholera toxin B/ganglioside GM_(1), antidinitrophenyl (DNP) antibody/DNP, and NeutrAvidin/biotin protein-ligand systems were used to model multiple protein-ligand binding on the MLBAs. The multicomponent patterned bilayers were functionalized with GM_(1), DNP, and biotin lipids, and binding curves was generated by recording surface fluorescence versus increasing concentration of membrane bound ligands.
机译:我们已经开发了一种使用3D微流控系统创建微模式脂质双层阵列(MLBA)的新方法。使用连续流动微量点样仪将一系列液体脂质膜图案化到玻璃基板上。荧光显微镜实验用于验证在玻璃基板上双层结构的形成。光漂白实验后的荧光恢复表明,双层膜的流动性得以保持,同时被单独固定在基质上。阵列内双层形成的可再现性由膜荧光与融合到表面之前掺入囊泡中的罗丹明官能化脂质的摩尔百分比的线性响应证实。 MLBAs的高度可定制性质已证明,利用三种不同的荧光标记脂质来生成多组分脂质阵列。最后,霍乱毒素B /神经节苷脂GM_(1),抗二硝基苯基(DNP)抗体/ DNP和NeutrAvidin /生物素蛋白-配体系统用于模拟MLBAs上的多种蛋白-配体结合。用GM_(1),DNP和生物素脂质对多组分图案化的双层进行功能化,并通过记录表面荧光对膜结合配体浓度的增加来生成结合曲线。

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