Biomicrofluidics. 2011 Mar 30;5(1):13410. doi: 10.1063/1.3528237.
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.
微型化诊断领域的发展受到缺乏预处理手段的阻碍,这些手段能够以高通量的方式处理小体积样本,用于检测低浓度分析物。本研究提出了一种新颖、高效的从生物流体中提取低分子量(LMW)蛋白质的方法,以标准蛋白质混合物为例,使用集成微流控系统。我们将带有微流道的聚二甲基硅氧烷层键合到具有明确纳米孔的二氧化硅基底上。通过快速、压力驱动的分级步骤,该系统利用二氧化硅纳米孔的尺寸排阻特性去除高分子量蛋白质,同时分离和富集生物样品中存在的低分子量蛋白质。微流控组件的引入具有许多重要优势,如高重现性、简单的用户界面、受控环境、处理小体积样本的能力以及精确的定量。该解决方案简化了高通量蛋白质组学研究的许多方面,并可能在临床诊断和即时检测中得到广泛接受和应用。