Fouqué B, Brachet A G, Gétin S, Pégon P, Obeïd P, Delapierre G, Chatelain F
CEA, DSV/DRDC/Biopuces, Grenoble F-38054, France.
Biosens Bioelectron. 2007 Apr 15;22(9-10):2151-7. doi: 10.1016/j.bios.2006.09.036. Epub 2006 Nov 7.
Today, microarray fluorescence detection is still limited because a great proportion of hybrids remain undetectable. In this paper we describe sol-gel optical multilayers (stacks of low- and high-index layers) deposited on glass slides which increase the fluorescence of DNA microarrays and favour the detection of fluorescent targets. An alternative to the expensive and time-consuming physical vapour deposition technology is proposed. It is a low-cost sol-gel coating of glass slides, each layer being made by "dipping" (alternatively in SiO2 or TiO2 solutions), "draining and drying". After the selection of the best surface layer of the substrates, the multilayer mirrors modelled for one (Cy3) or two (Cy3 and Cy5) fluorophores are spotted with a series of Yeast probes and compared to similar microarrays on standard glass slides through hybridisation experiments. The fluorescence images of the mirrors show increased signals for all the probes. The enhancement factors determined for Cy3 and for Cy3/Cy5 mirrors (10-12 and 4-5, respectively) are consistent with the initial modelling. This allows the assessment of the basal expression levels of Yeast low-expressed genes. Moreover, these substrates show a noticeable increase in sensitivity for induction/repression ratio measurements in differential gene expression experiments. So, they could be considered as promising tools for the analysis of small biological samples.
如今,微阵列荧光检测仍受到限制,因为很大一部分杂交体仍无法检测到。在本文中,我们描述了沉积在载玻片上的溶胶 - 凝胶光学多层膜(低折射率和高折射率层的堆叠),它可增强DNA微阵列的荧光并有利于荧光靶标的检测。本文提出了一种替代昂贵且耗时的物理气相沉积技术的方法。它是一种载玻片的低成本溶胶 - 凝胶涂层,每层通过“浸渍”(交替浸入SiO2或TiO2溶液中)、“沥干和干燥”制成。在选择了最佳的基底表面层后,针对一种(Cy3)或两种(Cy3和Cy5)荧光团建模的多层反射镜用一系列酵母探针进行点样,并通过杂交实验与标准载玻片上的类似微阵列进行比较。反射镜的荧光图像显示所有探针的信号都增强了。为Cy3和Cy3/Cy5反射镜确定的增强因子(分别为10 - 12和4 - 5)与初始建模一致。这使得能够评估酵母低表达基因的基础表达水平。此外,这些基底在差异基因表达实验中对诱导/抑制比测量的灵敏度有显著提高。因此,它们可被视为分析小生物样本的有前景的工具。