Department of Bioengineering, 1304 W. Springfield Ave., University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
Anal Chem. 2010 Aug 15;82(16):6854-61. doi: 10.1021/ac100841d.
DNA microarrays are used to profile changes in gene expression between samples in a high-throughput manner, but measurements of genes with low expression levels can be problematic with standard microarray substrates. In this work, we expand the detection capabilities of a standard microarray experiment using a photonic crystal (PC) surface that enhances fluorescence observed from microarray spots. This PC is inexpensively and uniformly fabricated using a nanoreplica molding technique, with very little variation in its optical properties within- and between-devices. By using standard protocols to process glass microarray substrates in parallel with PCs, we evaluated the impact of this substrate on a one-color microarray experiment comparing gene expression in two developmental stages of Glycine max. The PCs enhanced the signal-to-noise ratio observed from microarray spots by 1 order of magnitude, significantly increasing the number of genes detected above substrate fluorescence noise. PC substrates more than double the number of genes classified as differentially expressed, detecting changes in expression even for low expression genes. This approach increases the dynamic range of a surface-bound fluorescence-based assay to reliably quantify small quantities of DNA that would be impossible with standard substrates.
DNA 微阵列用于以高通量方式分析样品之间基因表达的变化,但用标准微阵列基质测量低表达水平的基因可能会有问题。在这项工作中,我们使用光子晶体 (PC) 表面扩展了标准微阵列实验的检测能力,该表面增强了从微阵列斑点观察到的荧光。这种 PC 是使用纳米复制成型技术廉价且均匀地制造的,其在设备内和设备之间的光学性能变化很小。通过使用标准协议来并行处理玻璃微阵列基质和 PC,我们评估了这种基质对比较 Glycine max 两个发育阶段基因表达的双色微阵列实验的影响。PC 将从微阵列斑点观察到的信噪比提高了 1 个数量级,显著增加了检测到的高于基质荧光噪声的基因数量。PC 基质使被分类为差异表达的基因数量增加了两倍以上,甚至可以检测到低表达基因的表达变化。这种方法增加了基于表面结合荧光的测定法的动态范围,从而能够可靠地定量分析用标准基质不可能进行定量的少量 DNA。