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DNA Nanotweezers with Hydrolytic Activity for Enzyme-Free and Sensitive Detection of Fusion Gene via Logic Operation

机译:具有水解活性的DNA纳米镊子可通过逻辑操作无酶灵敏地检测融合基因

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摘要

Gene fusion is a molecular event occurring in cellular proliferation and differentiation, and the occurrence of irregular fusion gene results in various malignant diseases. So, sensing fusion gene with high performance is an important task for integrating individual disease information. Here, we proposed a nonenzymatic and high-throughput fluorescent assay system for the detection of fusion gene by employing DNA nanotweezers with hydrolytic activity. This tweezer was assembled by three single-stranded DNAs and engineered with sensing elements and reporting subunits. In the absence of the fusion gene, the engineered tweezer remained opened and inactive which led to no signal output. However, the addition of fusion genes would cause structure alterations of the tweezer from open to close and further DNAzyme activation with the assembly of two reporting subunits. Then, the activated DNAzyme catalyzed fluorescence substrates for signal conversion. Taking BCR/ABL fusion gene as an example, the tweezer-based assay system showed not only excellent distinguishing capability towards different input targets but also high sensitivity with a detection limit of 5.29 pM. In addition to good detection performance, this system was simple and enzyme-free, offering a powerful nanometer tool as a smart nanodevice for sensing fusion detection.
机译:基因融合是发生在细胞增殖和分化中的分子事件,不规则融合基因的出现导致各种恶性疾病。因此,高性能的融合基因检测是整合单个疾病信息的重要任务。在这里,我们提出了一种非酶和高通量的荧光检测系统,用于通过使用具有水解活性的DNA纳米镊子来检测融合基因。该镊子由三个单链DNA组装而成,并经过了传感元件和报告亚基的改造。在没有融合基因的情况下,工程镊子保持打开状态且不活动,这导致没有信号输出。然而,融合基因的添加将导致镊子的结构从打开到闭合的改变,并伴随两个报告亚基的组装而进一步激活DNAzyme。然后,活化的DNA核酶催化荧光底物用于信号转换。以BCR / ABL融合基因为例,基于镊子的测定系统不仅显示出对不同输入目标的出色区分能力,而且还显示出5.29 pM的高灵敏度。除了良好的检测性能外,该系统还简单且无酶,提供了功能强大的纳米工具,可作为智能纳米设备进行融合检测。

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