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利用未经修饰的金纳米粒子和目标物催化发夹组装扩增实现具有可调动态范围的超灵敏 DNA 可视化检测。

Ultrasensitive visual detection of DNA with tunable dynamic range by using unmodified gold nanoparticles and target catalyzed hairpin assembly amplification.

机构信息

Science and Technology on Surface Physics and Chemistry Laboratory, P.O.Box No.9-35, Jiangyou City, Sichuan 621908, PR China.

Science and Technology on Surface Physics and Chemistry Laboratory, P.O.Box No.9-35, Jiangyou City, Sichuan 621908, PR China.

出版信息

Biosens Bioelectron. 2016 Mar 15;77:421-7. doi: 10.1016/j.bios.2015.09.065. Epub 2015 Sep 30.

Abstract

A simple and novel strategy for enzyme-free ultrasensitive DNA detection platform has been present here based on gold nanoparticles (AuNPs) colorimetry and target catalyzed hairpin assembly amplification. Three hairpin auxiliary probes (H1, H2, and H3) are designed with signal-stranded DNA (ssDNA) sticky ends which could effectively stabilize AuNPs against salt-induced aggregation. However, a cascade of assembly steps with H1, H2, and H3 are activated in the presence of the target DNA, followed by a disassembly step in which H3 displaces the target DNA from the complex, freeing the target DNA to catalyze the self-assembly of additional branched junctions. The formed branched junction consisted with dsDNA is stiffer, and cannot prevent salt-induced AuNPs aggregation, corresponding to a red-to-blue color change. The result can be read out by naked eyes or UV-vis spectrometer. The detection limit of this method is 0.1 pM by naked eyes, and this result is comparable or even better than enzyme or hybridization chain reaction (HCR) based amplification AuNPs colorimetric assays. Moreover, the dynamic range of sensor could be tuned by using different concentration of hairpins. Importantly, this strategy provides a versatile ultrasensitive detection platform for the DNA and related filed targets including metal ions, small molecules, proteins, cells et al. by combining with specific DNAzymes and aptamers.

摘要

这里提出了一种基于金纳米粒子(AuNPs)比色法和目标催化发夹组装扩增的简单新颖的无酶超灵敏 DNA 检测平台策略。设计了三个带有信号链 DNA(ssDNA)粘性末端的发夹辅助探针(H1、H2 和 H3),可以有效地稳定 AuNPs 免受盐诱导的聚集。然而,在存在目标 DNA 的情况下,通过一系列的组装步骤激活 H1、H2 和 H3,随后是 H3 将目标 DNA 从复合物中置换出来的解组装步骤,从而释放目标 DNA 以催化额外分支结的自组装。形成的包含 dsDNA 的分支结更硬,不能防止盐诱导的 AuNPs 聚集,对应于红色到蓝色的颜色变化。结果可以通过肉眼或紫外-可见分光光度计读出。通过肉眼,该方法的检测限可达 0.1 pM,这一结果可与基于酶或杂交链式反应(HCR)的扩增 AuNPs 比色测定相媲美,甚至更好。此外,通过使用不同浓度的发夹可以调整传感器的动态范围。重要的是,通过与特定的 DNA 酶和适体结合,该策略为 DNA 及相关领域的目标(包括金属离子、小分子、蛋白质、细胞等)提供了一种通用的超灵敏检测平台。

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