Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT, USA.
Electrophoresis. 2009 Dec;30(24):4230-6. doi: 10.1002/elps.200900349.
Microchip CE of proteins labeled either off- or on-chip with the "chameleon" CE dye 503 using poly(methyl methacrylate) microchips is presented. A simple dynamic coating using the cationic surfactant CTAB prevented nonspecific adsorption of protein and dye to the channel walls. The labeling reactions for both off- and on-chip labeling proceeded at room temperature without requiring heating steps. In off-chip labeling, a 9 ng/mL concentration detection limit for BSA, corresponding to a approximately 7 fg (100 zmol) mass detection limit, was obtained. In on-chip tagging, the free dye and protein were placed in different reservoirs of the microchip, and an extra incubation step was not needed. A 1 microg/mL concentration detection limit for BSA, corresponding to a approximately 700 fg (10 amol) mass detection limit, was obtained from this protocol. The earlier elution time of the BSA peak in on-chip labeling resulted from fewer total labels on each protein molecule. Our on-chip labeling method is an important part of automation in miniaturized devices.
本文介绍了一种使用聚甲基丙烯酸甲酯微芯片,对在芯片上或在芯片外标记的蛋白质进行微芯片毛细管电泳(CE)的方法。通过使用阳离子表面活性剂 CTAB 进行简单的动态涂层处理,可以防止蛋白质和染料非特异性地吸附到通道壁上。无论是在芯片外还是在芯片内进行标记,标记反应都可以在室温下进行,无需加热步骤。在芯片外标记中,获得了对 BSA 的 9ng/mL 浓度检测限,相当于大约 7fg(100zmol)的质量检测限。在芯片内标记中,将游离染料和蛋白质分别放置在微芯片的不同储液器中,无需额外的孵育步骤。从该方案中获得了对 BSA 的 1μg/mL 浓度检测限,相当于大约 700fg(10amol)的质量检测限。在芯片内标记中,BSA 峰的洗脱时间较早,这是因为每个蛋白质分子上的总标记数量较少。我们的芯片内标记方法是小型化设备自动化的重要组成部分。