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A Plug-Based Microfluidic System for Dispensing Lipidic Cubic Phase (LCP) Material Validated by Crystallizing Membrane Proteins in Lipidic Mesophases

机译:一种基于塞子的微流体系统,用于分配脂质立方相(LCP)材料,该材料通过使脂质中间相中的膜蛋白结晶而验证

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摘要

This article presents a plug-based microfluidic system to dispense nanoliter-volume plugs of lipidic cubic phase (LCP) material and subsequently merge the LCP plugs with aqueous plugs. This system was validated by crystallizing membrane proteins in lipidic mesophases, including LCP. This system allows for accurate dispensing of LCP material in nanoliter volumes, prevents inadvertent phase transitions that may occur due to dehydration by enclosing LCP in plugs, and is compatible with the traditional method of forming LCP material using a membrane protein sample, as shown by the successful crystallization of bacteriorhodopsin from Halobacterium salinarum. Conditions for the formation of LCP plugs were characterized and presented in a phase diagram. This system was also implemented using two different methods of introducing the membrane protein: (1) the traditional method of generating the LCP material using a membrane protein sample and (2) post LCP-formation incorporation (PLI), which involves making LCP material without protein, adding the membrane protein sample externally to the LCP material, and allowing the protein to diffuse into the LCP material or into other lipidic mesophases that may result from phase transitions. Crystals of bacterial photosynthetic reaction centers from Rhodobacter sphaeroides and Blastochloris viridis were obtained using PLI. The plug-based, LCP-assisted microfluidic system, combined with the PLI method for introducing membrane protein into LCP, should be useful for minimizing consumption of samples and broadening the screening of parameter space in membrane protein crystallization.
机译:本文介绍了一种基于塞子的微流体系统,用于分配纳升体积的脂质立方相(LCP)材料塞,然后将LCP塞子与水性塞子合并。该系统通过使包括LCP在内的脂质中间相中的膜蛋白结晶而得到验证。该系统允许以纳升体积精确分配LCP材料,防止由于将LCP封闭在塞子中而由于脱水而发生的意外相变,并且与使用膜蛋白样品形成LCP材料的传统方法兼容,如成功从盐杆菌中结晶出细菌视紫红质。表征了LCP塞的形成条件,并以相图形式表示。该系统还使用两种不同的引入膜蛋白的方法来实现:(1)使用膜蛋白样品生成LCP材料的传统方法,以及(2)LCP形成后掺入(PLI),这涉及在不使用LCP材料的情况下制备LCP材料。蛋白质,将膜蛋白质样品从外部添加到LCP材料中,并允许蛋白质扩散到LCP材料或其他可能由相变产生的脂质中间相中。使用PLI从球形球形红细菌和绿色拟杆菌中获得细菌光合作用反应中心的晶体。基于插头的,LCP辅助的微流体系统,与将膜蛋白引入LCP的PLI方法相结合,对于最小化样品消耗和拓宽膜蛋白结晶参数空间的筛选应该是有用的。

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