Department of Applied Physics, Graduate School of Engineering, Osaka University, 2-1 Yamada-Oka, Suita, Osaka 565-0871, Japan.
Anal Chim Acta. 2010 Feb 19;661(1):111-6. doi: 10.1016/j.aca.2009.12.006. Epub 2009 Dec 14.
In this report, Au-coated nanostructured biochip with functionalized thiolated primers on its surface is developed for label-free and real-time optical detection of polymerase chain reaction (PCR). A PCR chamber of 150 microm in thickness containing Au-coated nanostructured substrate in the bottom layer was bordered with SU-8 100 walls. After immobilization of 5'-thiolated primers on the surface, simultaneous DNA amplification and detection were performed without any labeled molecules via the relative reflected intensity (RRI) of Au-coated nanostructured substrate. When human genomic DNA at several concentrations of 0.2, 0.5 and 1 ng microL(-1) was included in the initial DNA samples, the increases in the RRI peak values were clearly observed with the increasing PCR cycle numbers. We found that the starting point of the optical signal, which was divergent from the background in our PCR biochip, was around 3-4 cycles, much lower than that of the fluorescent real-time PCR analysis (around 23-25 cycles). Our proposed PCR device using Au-coated nanostructured substrate holds noteworthy promise for rapid, label-free and real-time DNA detection for point-of-care testing (POCT) applications.
本报告开发了一种表面带有功能化硫醇化引物的金纳米结构生物芯片,用于无标记实时光学检测聚合酶链反应(PCR)。PCR 室的厚度为 150 微米,底部层为带有金纳米结构基底的 SU-8 100 壁。表面固定 5′-硫醇化引物后,通过金纳米结构基底的相对反射强度(RRI),无需任何标记分子即可进行同时的 DNA 扩增和检测。当初始 DNA 样本中包含浓度为 0.2、0.5 和 1ngμL-1 的人基因组 DNA 时,随着 PCR 循环数的增加,RRI 峰值的增加明显可见。我们发现,在我们的 PCR 生物芯片中,与背景不同的光学信号起点约为 3-4 个循环,远低于荧光实时 PCR 分析(约 23-25 个循环)。我们提出的使用金纳米结构基底的 PCR 装置有望用于即时护理测试(POCT)应用的快速、无标记和实时 DNA 检测。