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25 second cocaine sensing by membrane protein channel integrated in a microfluidic device

机译:通过集成在微流控设备中的膜蛋白通道进行25秒可卡因感测

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This paper describes a cocaine sensing using a membrane protein channel integrated in a microfluidic device (Figure 1). Protein channel (1.5 nm dia.) was reconstituted in planar lipid bilayers (BLMs) spanning at nanometer-sized parylene nanopore (400 nm dia., Figure 1b). DNA dissolved in solution can be driven through an alpha-hemolysin (αHL) channel by an applied electric field (Figure 1c left), and it was recognized as single molecular level by monitoring the channel currents. It was revealed in this study that a cocaine was discriminated by the protein channel as changing the structure from a cocaine molecule to a cocaine aptamer complex as shown Figure 1c right. We demonstrated that the cocaine aptamer can be sensed for only 25 second in the 3D microfluidic device.
机译:本文介绍了使用集成在微流控设备中的膜蛋白通道进行可卡因感测的方法(图1)。蛋白质通道(直径1.5 nm)在平面脂质双层(BLM)中重建,该脂质跨膜跨越纳米级聚对二甲苯纳米孔(直径400 nm,图1b)。溶解在溶液中的DNA可以通过施加的电场通过α-溶血素(αHL)通道驱动(图1c左),通过监测通道电流可以将其识别为单分子水平。在这项研究中发现,可卡因通过蛋白质通道区分为可卡因分子从可卡因分子变为可卡因适体复合物的结构,如图1c右所示。我们证明了在3D微流控设备中可卡因适体仅能感测25秒。

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