The University of Hull, Department of Chemistry, Cottingham Road, Hull HU67RX, UK.
Biosens Bioelectron. 2010 May 15;25(9):2172-6. doi: 10.1016/j.bios.2010.01.034. Epub 2010 Feb 4.
DNA hybridisation is an important tool for bioanalytical research and clinical diagnostics; conventional methods, however, require long incubation times and numerous washing steps, rendering the procedure time consuming and labour intensive. In this paper, we report on a rapid method for DNA hybridisation and isolation within a microfluidic device, where all reaction and washing steps are performed in continuous flow in an automated fashion within less than two minutes. Magnetic particles were used as a solid support and manipulated through laminar flow streams containing reagents and buffers by means of an external magnet. Thus, hybridisation, washing, intercalation, fluorescence detection and isolation were performed in continuous flow on the surface of the particles. Initially, the sensitivity of the system was investigated for a one-step DNA hybridisation of Alexa Fluor 555 labelled target DNA to a capture probe immobilised on the particle surface. Hybridisation and washing steps were performed in half a minute and target DNA was readily detected down to 20 nmol L(-1). Then a two-step assay, label-free DNA hybridisation followed by intercalation with PicoGreen was performed. All reaction and washing steps were carried out in continuous flow with a total assay time of about 1 min. This is a significant reduction in procedural time compared to conventional methods and opens the door for developing fully automated continuous flow integrated DNA analysis platforms.
DNA 杂交是生物分析研究和临床诊断的重要工具;然而,传统方法需要长时间的孵育和多次洗涤步骤,使得该过程耗时且劳动强度大。在本文中,我们报告了一种在微流控设备内快速进行 DNA 杂交和分离的方法,其中所有的反应和洗涤步骤都在不到两分钟的时间内以自动化的方式在连续流中进行。磁性颗粒被用作固相支持,并通过外部磁铁在含有试剂和缓冲液的层流流中进行操纵。因此,在颗粒表面上以连续流的方式进行杂交、洗涤、嵌入、荧光检测和分离。最初,我们研究了该系统的灵敏度,用于将 Alexa Fluor 555 标记的靶 DNA 与固定在颗粒表面上的捕获探针进行一步 DNA 杂交。杂交和洗涤步骤在半分钟内完成,可轻松检测到低至 20 nmol L(-1)的靶 DNA。然后进行了两步检测,无标记 DNA 杂交,然后用 PicoGreen 进行嵌入。所有的反应和洗涤步骤都在连续流中进行,总检测时间约为 1 分钟。与传统方法相比,这大大减少了操作时间,为开发全自动连续流集成 DNA 分析平台开辟了道路。