Department of Chemistry, University of Michigan, 930 N. University Ave, Ann Arbor, MI, 48109-1055, USA.
Department of Pharmacology, University of Michigan, 1150 W. Medical Center Dr, Ann Arbor, MI, 48109-5632, USA.
Anal Bioanal Chem. 2019 Sep;411(23):6155-6163. doi: 10.1007/s00216-019-02006-7. Epub 2019 Jul 13.
Electrophoresis has demonstrated utility as tool for screening of small molecule modulators of protein-protein interactions and enzyme targets. Screening of large chemical libraries requires high-throughput separations. Such fast separation can be accessed by microchip electrophoresis. Here, microchip gel electrophoresis separations of proteins are achieved in 2.6 s with 1200 V/cm and 3-mm separation lengths. However, such fast separations can still suffer from limited overall throughput from sample introduction constraints. Automated introduction of microfluidic droplets has been demonstrated to overcome this limitation. Most devices for coupling microfluidic droplets to microchip electrophoresis are only compatible with free-solution separations. Here, we present a device that is compatible with coupling droplets to gel and free-solution electrophoresis. In this device, automated sample introduction is based on a novel mechanism of carrier phase separation using the difference in density of the carrier phase and the running buffer. This device is demonstrated for microchip gel electrophoresis and free-solution electrophoresis separations of protein-protein interaction and enzyme samples, respectively. Throughputs of about 10 s per sample are achieved and over 1000 separations are demonstrated without reconditioning of the device. Graphical abstract.
电泳已被证明是筛选小分子蛋白-蛋白相互作用调节剂和酶靶标的工具。对大型化学库的筛选需要高通量分离。微芯片电泳可以实现这种快速分离。在这里,在 1200 V/cm 和 3-mm 分离长度下,通过微芯片凝胶电泳在 2.6 s 内实现蛋白质的分离。然而,这种快速分离仍然可能受到样品引入限制的整体通量限制。已经证明自动化引入微流滴可以克服这一限制。大多数用于将微流滴与微芯片电泳耦合的设备仅与游离溶液分离兼容。在这里,我们提出了一种与胶和游离溶液电泳结合使用的设备。在该设备中,自动化进样是基于使用载体相和运行缓冲液之间的密度差的载体相分离的新机制。该设备分别用于微芯片凝胶电泳和蛋白质-蛋白质相互作用和酶样品的游离溶液电泳分离。每个样品的通量约为 10 秒,在不重新调节设备的情况下,可实现超过 1000 次分离。