首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >A label-free DNAzyme fluorescence biosensor for amplified detection of Pb2+-based on cleavage-induced G-quadruplex formation
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A label-free DNAzyme fluorescence biosensor for amplified detection of Pb2+-based on cleavage-induced G-quadruplex formation

机译:基于裂解诱导的G-四链体形成的无标记DNAzyme荧光生物传感器,用于扩增检测Pb2 +。

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摘要

DNAzyme-based catalytic beacons have been widely studied for both in vivo and in vitro molecular detection. However, only a few label-free catalytic beacons with excellent analytical performance have been reported so far. In this work, by combining a catalytic DNAzyme for amplified sensing through enzymatic turnover with cleavage-induced G-quadruplex formation, a label-free DNAzyme biosensor was developed for amplified "turn-on" fluorescence detection of Pb2+ with a detection limit of 3 nM. The method is very competitive compared to many other labeled or label-free methods with or without signal amplification. Due to the inherent specificity of the GR-5 DNAzyme, the method also exhibits excellent selectivity. This biosensor successfully detected Pb2+ in river water samples with high sensitivity and selectivity. Such a method might provide a universal DNAzyme-based sensing platform for sensitive detection of various targets both in environmental and biomedical fields. (C) 2015 Elsevier B.V. All rights reserved.
机译:基于DNAzyme的催化信标已广泛用于体内和体外分子检测。但是,到目前为止,仅报道了少数具有出色分析性能的无标记催化信标。在这项工作中,通过将催化性DNA酶用于通过酶促更新进行扩增感测与裂解诱导的G-四链体形成相结合,开发了一种无标记的DNAzyme生物传感器,用于扩增Pb2 +的“开启”荧光检测,检测极限为3 nM 。与许多其他带信号放大或不带信号放大的标记或无标记方法相比,该方法极具竞争力。由于GR-5 DNAzyme的固有特异性,该方法还具有出色的选择性。该生物传感器以高灵敏度和高选择性成功地检测了河水样品中的Pb2 +。这样的方法可能会提供一个基于DNAzyme的通用传感平台,用于环境和生物医学领域中各种目标的灵敏检测。 (C)2015 Elsevier B.V.保留所有权利。

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