Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin 300072, China.
Anal Chem. 2011 Oct 1;83(19):7500-6. doi: 10.1021/ac201755x. Epub 2011 Sep 14.
A simple, rapid, and sensitive method for visual detection of sequence-specific DNA was developed using hairpin DNA as the recognition element and hydroxylamine-enlarged gold nanoparticles (Au-NPs) as the signal producing component. In the assay, we employed a hairpin DNA probe dually labeled with amine and biotin at the 5'- and 3'-end, respectively. The probe was coupled with reactive N-oxysuccinnimide in a DNA-bind 96-well plate. Without the target DNA, the immobilized hairpin probe was in a "closed" state, which kept the streptavidin-gold off the biotin. The hybridization between the loop sequence and the target broke the short stem duplex upon approaching the target DNA. Consequently, biotin was forced away from the 96-well plate surface and available for conjugation with the streptavidin-gold. The hybridization could be detected visually after the HAuCl(4)-NH(2)OH redox reaction catalyzed by the Au-NPs. Under the optimized conditions, the visual DNA sensor could detect as low as 100 amol of DNA targets with excellent differentiation ability and even a single-base mismatch.
一种简单、快速、灵敏的用于视觉检测序列特异性 DNA 的方法已经开发出来,使用发夹 DNA 作为识别元件和羟胺放大的金纳米粒子 (Au-NPs) 作为信号产生组件。在该测定中,我们采用了分别在 5'和 3'末端标记有胺和生物素的发夹 DNA 探针。探针与 DNA 结合在 96 孔板中的反应性 N-羟基琥珀酰亚胺结合。没有目标 DNA 时,固定化的发夹探针处于“闭合”状态,使链霉亲和素-金远离生物素。当接近目标 DNA 时,环序列与目标之间的杂交会破坏短茎双链。因此,生物素被迫离开 96 孔板表面,并可与链霉亲和素-金结合。在 Au-NPs 催化的 HAuCl(4)-NH(2)OH 氧化还原反应后,可以进行可视化检测。在优化条件下,该视觉 DNA 传感器可以检测低至 100 amol 的 DNA 靶标,具有出色的区分能力,甚至可以检测到单个碱基错配。