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Microfluidic enrichment of small proteins from complex biological mixture on nanoporous silica chip

机译:纳米多孔二氧化硅芯片上复杂生物混合物中小蛋白质的微流富集

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摘要

The growing field of miniaturized diagnostics is hindered by a lack of pre-analysis treatments that are capable of processing small sample volumes for the detection of low concentration analytes in a high-throughput manner. This letter presents a novel, highly efficient method for the extraction of low-molecular weight (LMW) proteins from biological fluids, represented by a mixture of standard proteins, using integrated microfluidic systems. We bound a polydimethylsiloxane layer patterned with a microfluidic channel onto a well-defined nanoporous silica substrate. Using rapid, pressure-driven fractionation steps, this system utilizes the size-exclusion properties of the silica nanopores to remove high molecular weight proteins while simultaneously isolating and enriching LMW proteins present in the biological sample. The introduction of the microfluidic component offers important advantages such as high reproducibility, a simple user interface, controlled environment, the ability to process small sample volumes, and precise quantification. This solution streamlines high-throughput proteomics research on many fronts and may find broad acceptance and application in clinical diagnostics and point of care detection.
机译:由于缺乏能够进行小样本量高通量检测低浓度分析物的预分析处理,阻碍了小型化诊断技术的发展。这封信提出了一种使用集成的微流体系统从生物流体中提取低分子量(LMW)蛋白的新方法,该蛋白以标准蛋白的混合物为代表。我们将图案化有微流体通道的聚二甲基硅氧烷层结合到定义明确的纳米多孔二氧化硅基质上。通过快速,压力驱动的分级分离步骤,该系统利用了二氧化硅纳米孔的尺寸排阻特性来去除高分子量蛋白质,同时分离并富集了生物样品中存在的LMW蛋白质。微流体组分的引入提供了重要的优势,例如高重现性,简单的用户界面,受控的环境,处理小样品量的能力以及精确的定量。该解决方案简化了许多领域的高通量蛋白质组学研究,并可能在临床诊断和护理点检测中获得广泛的接受和应用。

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