Institute of Fluorescence, University of Maryland Baltimore County, 701 East Pratt Street, Baltimore, MD 21202, USA.
J Immunol Methods. 2011 Mar 7;366(1-2):1-7. doi: 10.1016/j.jim.2010.12.002. Epub 2010 Dec 13.
For analyses of DNA fragment sequences in solution we introduce a 2-color DNA assay, utilizing a combination of the Metal-Enhanced Fluorescence (MEF) effect and microwave-accelerated DNA hybridization. The assay is based on a new "Catch and Signal" technology, i.e. the simultaneous specific recognition of two target DNA sequences in one well by complementary anchor-ssDNAs, attached to silver island films (SiFs). It is shown that fluorescent labels (Alexa 488 and Alexa 594), covalently attached to ssDNA fragments, play the role of biosensor recognition probes, demonstrating strong response upon DNA hybridization, locating fluorophores in close proximity to silver NPs, which is ideal for MEF. Subsequently the emission dramatically increases, while the excited state lifetime decreases. It is also shown that 30s microwave irradiation of wells, containing DNA molecules, considerably (~1000-fold) speeds up the highly selective hybridization of DNA fragments at ambient temperature. The 2-color "Catch and Signal" DNA assay platform can radically expedite quantitative analysis of genome DNA sequences, creating a simple and fast bio-medical platform for nucleic acid analysis.
为了分析溶液中的 DNA 片段序列,我们引入了一种双色 DNA 分析方法,利用金属增强荧光(MEF)效应和微波加速 DNA 杂交。该方法基于一种新的“捕获和信号”技术,即在一个孔中同时通过互补的锚定 ssDNA 特异性识别两个靶 DNA 序列,这些 ssDNA 连接到银岛薄膜(SiFs)上。结果表明,共价连接到 ssDNA 片段上的荧光标记物(Alexa 488 和 Alexa 594)作为生物传感器识别探针,在 DNA 杂交时表现出强烈的响应,将荧光团定位在银纳米颗粒附近,这非常适合 MEF。随后,发射强度显著增加,而激发态寿命降低。实验还表明,对含有 DNA 分子的孔进行 30 秒微波辐射,可以大大(约 1000 倍)加快在环境温度下 DNA 片段的高度选择性杂交。这种双色“捕获和信号”DNA 分析平台可以极大地加速基因组 DNA 序列的定量分析,为核酸分析创建了一个简单快速的生物医学平台。