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Poly (dimethylsiloxane)-Based Protein Preconcentration Using a Nanogap Generated by Junction Gap Breakdown

机译:结缝击穿产生的纳米间隙使基于聚二甲基硅氧烷的蛋白质富集

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摘要

Simple and efficient sample concentration tools are thekey to the application of proteomics in a biological system. In this paper, we developed a method to realize a nanofluidic preconcentrator on a poly(dimethylsiloxane) (PDMS)-based microfluidic channel. The originality of our preconcentration device is the simple nanogap formation using the junction gap breakdown phenomenon between two PDMS microchannels, without using any photolithography and etching techniques. From the dc current measurement, we confirm that the nanogap formed between two microchannel junctions with approximately 80 nm depth. Using this device, we achieve the concentration volume of beta-phycoerythrin protein as high as 70 pL, which is 120-fold larger than that from our previous reports, with a concentration factor as high as 10~(4) within 1 h. Also we show the availability of protein preconcentration under several different buffers (phosphate, acetate) at several different pH values (pH 5 to pH 9).
机译:简单有效的样品浓缩工具是蛋白质组学在生物系统中应用的关键。在本文中,我们开发了一种在基于聚二甲基硅氧烷(PDMS)的微流体通道上实现纳米流体预浓缩器的方法。我们的预浓缩设备的独创性是利用两个PDMS微通道之间的结合间隙击穿现象,无需使用任何光刻和蚀刻技术即可形成简单的纳米间隙。从直流电流测量中,我们确认纳米间隙在两个深度约为80 nm的微通道结之间形成。使用该装置,我们可以使β-藻红蛋白的浓度达到70 pL,比以前的报道大120倍,并且在1小时内的浓度系数高达10〜(4)。我们还显示了在几种不同pH值(pH 5至pH 9)下,在几种不同缓冲液(磷酸盐,乙酸盐)下蛋白质预浓缩的可用性。

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