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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Toehold strand displacement-driven assembly of G-quadruplex DNA for enzyme-free and non-label sensitive fluorescent detection of thrombin
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Toehold strand displacement-driven assembly of G-quadruplex DNA for enzyme-free and non-label sensitive fluorescent detection of thrombin

机译:脚趾链置换驱动的G-四链体DNA组装,用于无酶和凝血酶的非标记敏感荧光检测

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摘要

Based on a new signal amplification strategy by the toehold strand displacement-driven cyclic assembly of G-quadruplex DNA, the development of an enzyme-free and non-label aptamer sensing approach for sensitive fluorescent detection of thrombin is described. The target thrombin associates with the corresponding aptamer of the partial dsDNA probes and liberates single stranded initiation sequences, which trigger the toehold strand displacement assembly of two G-quadruplex containing hairpin DNAs. This toehold strand displacement reaction leads to the cyclic reuse of the initiation sequences and the production of DNA assemblies with numerous G-quadruplex structures. The fluorescent dye, N-Methyl mesoporphyrin IX, binds to these G-quadruplex structures and generates significantly amplified fluorescent signals to achieve highly sensitive detection of thrombin down to 5 pM. Besides, this method shows high selectivity towards the target thrombin against other control proteins. The developed thrombin sensing method herein avoids the modification of the probes and the involvement of any enzyme or nanomaterial labels for signal amplification. With the successful demonstration for thrombin detection, our approach can be easily adopted to monitor other target molecules in a simple, low-cost, sensitive and selective way by choosing appropriate aptamer/ligand pairs. (C) 2014 Elsevier B.V. All rights reserved.
机译:基于新的信号放大策略,该信号放大策略由G-四链体DNA的脚趾链位移驱动的环状组装而来,描述了一种用于凝血酶敏感荧光检测的无酶,非标记适体传感方法的开发。目标凝血酶与部分dsDNA探针的相应适体缔合,并释放单链起始序列,从而触发两个含G-四链体的发夹DNA的鞋头链置换组装。该前额链置换反应导致起始序列的循环再利用以及具有许多G-四链体结构的DNA装配体的产生。荧光染料N-甲基中卟啉IX与这些G-四链体结构结合,并产生显着放大的荧光信号,以实现低至5 pM的凝血酶的高灵敏度检测。此外,该方法显示出针对靶凝血酶对其他对照蛋白的高选择性。本文开发的凝血酶感测方法避免了探针的修饰以及信号放大所需的任何酶或纳米材料标记物的参与。通过成功的凝血酶检测演示,通过选择合适的适体/配体对,我们的方法可以轻松地以简单,低成本,敏感和选择性的方式来监测其他目标分子。 (C)2014 Elsevier B.V.保留所有权利。

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