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靶向酶免双重扩增 DNA 电路用于快速信号放大。

Target-directed enzyme-free dual-amplification DNA circuit for rapid signal amplification.

机构信息

Fujian Key Laboratory of Functional Marine Sensing Materials, Center for Advanced Marine Materials and Smart Sensors, Minjiang University, Fuzhou 350108, P. R. China.

出版信息

J Mater Chem B. 2020 Dec 21;8(47):10770-10775. doi: 10.1039/d0tb02114h. Epub 2020 Nov 13.

Abstract

Dynamic DNA circuits have shown promising potential for amplified biosensing and bioengineering applications at the molecular level. Here, an enzyme-free, single-step and rapid signal amplification DNA circuit was developed by integrating target-directed entropy-driven catalysis (EDC) and hybridization chain reaction (HCR) for analysis of nucleic acids and small molecules. The target catalyzes the self-assembly of the EDC premade substrate complex and fuel strands to release the hidden amplicon trigger (T), which was encoded with trigger sequences for the downstream HCR circuit. The released T could motivate the successive cross-opening of HCR hairpins yielding long DNA nanowires and generated tremendously amplified fluorescence signals. Notably, this EDC-HCR circuit was driven by entropy without the requirement of any enzymes, thus greatly reducing the cost. The design of the hidden amplicon trigger (T) avoided the production of waste by-products and improved the reaction rate. Furthermore, as a modular circuit, we also demonstrated that our EDC-HCR cascade sensing system could be used as a versatile sensing platform for the highly sensitive and selective detection of other analysts, e.g. ATP in serum samples, through simply programming the reorganization sequences of the initiator. Therefore, the flexible and versatile EDC-HCR platform holds great potential in the fields of clinical diagnosis and biochemical analysis.

摘要

动态 DNA 电路在分子水平上的扩增生物传感和生物工程应用中显示出了巨大的潜力。在这里,通过整合靶标导向的熵驱动催化(EDC)和杂交链式反应(HCR),开发了一种无酶、单步、快速的信号放大 DNA 电路,用于分析核酸和小分子。靶标催化 EDC 预制底物复合物和燃料链的自组装,释放隐藏的扩增子触发物(T),T 被下游 HCR 电路的触发序列编码。释放的 T 可以激发 HCR 发夹的连续交联,产生极大放大的荧光信号。值得注意的是,该 EDC-HCR 电路由熵驱动,不需要任何酶,因此大大降低了成本。隐藏的扩增子触发物(T)的设计避免了产生废物副产物,并提高了反应速率。此外,作为一个模块化电路,我们还证明,我们的 EDC-HCR 级联传感系统可以通过简单地重组引发子的重组序列,作为一个通用的传感平台,用于高度敏感和选择性地检测其他分析物,例如血清样本中的 ATP。因此,灵活多样的 EDC-HCR 平台在临床诊断和生化分析领域具有巨大的潜力。

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