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Lipid Bilayer Formation by Contacting Monolayers in a Microfluidic Device for Membrane Protein Analysis

机译:通过在膜蛋白分析的微流控设备中接触单层脂质双层形成。

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Artificial planar lipid bilayers are a powerful tool for the functional study of membrane proteins, yet they have not been widely used due to their low stability and reproducibility. This paper describes an accessible method to form a planar lipid bilayer, simply by contacting two monolayers assembled at the interface between water and organic solvent in a microfluidic chip. The membrane of an organic solvent containing phospholipids at the interface was confirmed to be a bilayer by the capacitance measurement and by measuring the ion channel signal from reconstituted antibiotic peptides. We present two different designs for bilayer formation. One equips two circular wells connected, in which the water/solvent/water interface was formed by simply injecting a water droplet into each well. Another equips the cross-shaped microfluidic channel. In the latter design, formation of the interface at the sectional area was controlled by external syringe pumps. Both methods are extremely simple and reproducible, especially in microdevices, and will lead to automation and multiple bilayer formation for the high-throughput screening of membrane transport in physiological and pharmaceutical studies.
机译:人工平面脂质双层是膜蛋白功能研究的有力工具,但由于其低稳定性和可重复性,尚未得到广泛应用。本文介绍了一种简单的方法,即通过使组装在微流控芯片中水和有机溶剂之间的界面的两个单分子层接触,即可形成平面脂质双层。通过电容测量和通过测量来自重构的抗生素肽的离子通道信号,证实在界面处含有磷脂的有机溶剂的膜为双层。我们提出了两种不同的双层形成设计。一个人配备了两个相连的圆形井,其中只需将水滴注入每个井即可形成水/溶剂/水界面。另一个配备了十字形微流体通道。在后一种设计中,通过外部注射泵控制截面积界面的形成。两种方法都非常简单且可重现,尤其是在微型设备中,并且将导致自动化和多层双层形成,从而在生理和药物研究中对膜转运进行高通量筛选。

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