Hall Gordon H, Glerum D Moira, Backhouse Christopher J
Department of Electrical and Computer Engineering, University of Waterloo, ON, Canada.
Department of Biology, University of Waterloo, ON, Canada.
Electrophoresis. 2016 Feb;37(3):406-13. doi: 10.1002/elps.201500355. Epub 2015 Nov 24.
Electrophoretic separation of fluorescently end-labeled DNA after a PCR serves as a gold standard in genetic diagnostics. Because of their size and cost, instruments for this type of analysis have had limited market uptake, particularly for point-of-care applications. This might be changed through a higher level of system integration and lower instrument costs that can be realized through the use of LEDs for excitation and photodiodes for detection--if they provide sufficient sensitivity. Here, we demonstrate an optimized microchip electrophoresis instrument using polymeric fluidic chips with fluorescence detection of end-labeled DNA with a LOD of 0.15 nM of Alexa Fluor 532. This represents orders of magnitude improvement over previously reported instruments of this type. We demonstrate the system with an electrophoretic separation of two PCR products and their respective primers. We believe that this is the first LED-induced fluorescence microchip electrophoresis system with photodiode-based detection that could be used for standard applications of PCR and electrophoresis.
聚合酶链式反应(PCR)后对荧光末端标记的DNA进行电泳分离是基因诊断的金标准。由于此类分析仪器的尺寸和成本问题,其市场占有率有限,特别是在即时检测应用方面。通过更高水平的系统集成以及使用发光二极管(LED)进行激发和光电二极管进行检测来降低仪器成本,有可能改变这种情况——前提是它们能提供足够的灵敏度。在此,我们展示了一种优化的微芯片电泳仪器,该仪器使用聚合物微流控芯片,对末端标记的DNA进行荧光检测,对Alexa Fluor 532的检测限为0.15 nM。这比此前报道的此类仪器有了几个数量级的提升。我们通过对两种PCR产物及其各自引物进行电泳分离来展示该系统。我们认为这是首个基于光电二极管检测的LED诱导荧光微芯片电泳系统,可用于PCR和电泳的标准应用。