Hatakeyama Keiichi, Tanaka Tsuyoshi, Sawaguchi Masahiro, Iwadate Akihito, Mizutani Yasushi, Sasaki Kazuhiro, Tateishi Naofumi, Matsunaga Tadashi
Department of Biotechnology, Tokyo University of Agriculture and Technology, 2-24-16, Naka-cho, Koganei, 184-8588 Tokyo, Japan.
Lab Chip. 2009 Apr 21;9(8):1052-8. doi: 10.1039/b817427j. Epub 2009 Jan 21.
This work describes a novel microfluidic device using a thin film transistor (TFT) photosensor integrating a microfluidic channel, a DNA chip platform, and a photodetector for the discrimination of single nucleotide polymorphisms (SNPs). A DNA-arrayed TFT photosensor was used as a DNA chip platform and photo detecting device. Chemiluminescence was used for DNA sensing because chemiluminescence provides higher sensitivity and requires simpler instrumentation than fluorescence methods. The SNP of biotinylated target DNA was detected based on chemiluminescence by using horse radish peroxidase-conjugated streptavidin. The lower detection limit for a model biotinylated oligonucleotide (63-mer) was 0.5 nM, much lower than expected DNA concentrations in a practical application of this device. Furthermore, SNP detection in the aldehyde dehydrogenase 2 gene was successfully achieved using DNA-arrayed TFT photosensor without DNA extraction and DNA purification using PCR products. The assay was completed in less than one hour. Our technology will be a promising approach to developing a miniaturized, disposable DNA chip with high sensitivity.
这项工作描述了一种新型微流控装置,该装置使用薄膜晶体管(TFT)光电传感器,集成了微流控通道、DNA芯片平台和用于鉴别单核苷酸多态性(SNP)的光电探测器。一种DNA阵列TFT光电传感器被用作DNA芯片平台和光检测装置。化学发光用于DNA传感,因为与荧光方法相比,化学发光具有更高的灵敏度且所需仪器更简单。通过使用辣根过氧化物酶偶联的链霉亲和素,基于化学发光检测生物素化靶DNA的SNP。一种模型生物素化寡核苷酸(63聚体)的检测下限为0.5 nM,远低于该装置实际应用中预期的DNA浓度。此外,使用DNA阵列TFT光电传感器,无需对PCR产物进行DNA提取和纯化,成功实现了醛脱氢酶2基因中的SNP检测。该检测在不到一小时内完成。我们的技术将是开发一种具有高灵敏度的小型化、一次性使用DNA芯片的有前途的方法。