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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 >One DNA circle capture probe with multiple target recognition domains for simultaneous electrochemical detection of miRNA-21 and miRNA-155
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One DNA circle capture probe with multiple target recognition domains for simultaneous electrochemical detection of miRNA-21 and miRNA-155

机译:一种DNA圈捕获探针,具有多个目标识别结构域,用于同时电化学检测miRNA-21和miRNA-155

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摘要

In this work, a novel DNA circle capture probe with multiple target recognition domains was designed to develop an electrochemical biosensor for ultrasensitive detection of microRNA-21 (miRNA-21) and miRNA-155 simultaneously. The DNA circle capture probe was anchored at the top of the tetrahedron DNA nanostructure (TDN) to simultaneously recognize miRNA-21 and miRNA-155 through multiple target recognition domains under the assistance of Helper strands, which could trigger mimetic proximity ligation assay (mPLA) for capturing the beacons ferrocene (Fc)-A1 and methylene blue (MB)-A2 to achieve multiple miRNAs detection. In this way, the local reaction concentration could be enhanced and avoid the interference of various capture probes compared with the traditional multiplexed electrochemical biosensor with the use of different capture probes, resulting in the significantly improvement of detection sensitivity. As a result, this proposed biosensor showed wide linearity ranging from 0.1 fM to 10 nM with detection limits of miRNA-21 and miRNA-155 as 18.9 aM and 39.6 aM respectively, which also could be applied in the simultaneously detection of miRNA-21 and miRNA-155 from cancer cell lysates. The present strategy paved a new path in the design of capture probes for achieving more efficient and sensitive multiple biomarkers detections and possessed the potential applications in clinical diagnostic of diseases.
机译:在这项工作中,设计具有多个目标识别结构域的新型DNA圈捕获探针,用于同时开发用于微小RORNA-21(miRNA-21)和miRNA-155的超敏检测的电化学生物传感器。 DNA圆形捕获探针在四面体DNA纳米结构(TDN)的顶部锚定,以在辅助链的辅助下通过多个目标识别域同时识别miRNA-21和miRNA-155,这可能引发模拟接近连接测定(MPLA)用于捕获信标铁茂(FC)-A1和亚甲基蓝(MB)-A2以实现多种MiRNA检测。以这种方式,与使用不同的捕获探针的传统多重电化学生物传感器相比,可以提高局部反应浓度并避免各种捕获探针的干扰,从而显着提高了检测灵敏度的显着提高。结果,该拟议的生物传感器显示宽线性范围为0.1fm至10nm,分别为miRNA-21和miRNA-155的检测限,分别为18.9 AM和39.6μm,也可以应用于同时检测miRNA-21和来自癌细胞裂解物的miRNA-155。目前的策略铺设了一种在捕获探针设计中进行了一种新的路径,以实现更有效和敏感的多种生物标志物检测,并具有临床诊断中的潜在应用。

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