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A structure-switchable aptasensor for aflatoxin B1 detection based on assembly of an aptamer/split DNAzyme

机译:基于装配适体/分裂DNAzyme的用于黄曲霉毒素B1检测的结构可切换适体传感器

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摘要

An ultrasensitive, colorimetric and homogeneous strategy for aflatoxin B1 (AFB1) detection, which uses a DNA aptamer and two split DNAzyme halves, has been developed. Split halves of a hemin-binding DNAzymes is combined with an AFB1 aptamer to generate a homogeneous colorimetric sensor that undergoes an AFB1 induced DNA structural change. In the absence of AFB1, the split probes have peroxidase mimicking DNAzyme activity associated with catalysis of a color change reaction. Specific recognition of AFB1 by the aptamer component leads to structural deformation of the aptamer-DNAzyme complex, which causes splitting of the DNAzyme halves and a reduction in peroxidase mimicking activity. Therefore, a decrease of colorimetric signal arising from the catalytic process takes place upon in the presence of AFB1 in a concentration dependent manner in the 0.1-1.0 x 10(4) ng/mL range and with a colorimetric detection limit of 0.1 ng/mL. The new assay system exhibits high selectivity for AFB1 over other mycotoxins and can be employed detect the presence of AFB1 in ground corn samples. Overall, the strategy should serve as the basis for the development of rapid, simple and low-cost methods for detection of mycotoxins. (C) 2015 Elsevier B.V. All rights reserved.
机译:已经开发出一种超灵敏,比色和均相的黄曲霉毒素B1(AFB1)检测策略,该策略使用DNA适体和两个分裂的DNAzyme对分。将与血红素结合的DNAzymes的两半与AFB1适体结合,以产生均质的比色传感器,该传感器会经历AFB1诱导的DNA结构变化。在没有AFB1的情况下,分裂的探针具有过氧化物酶模拟DNA酶的活性,该酶与变色反应的催化有关。适体组分对AFB1的特异性识别导致适体-DNA酶复合物的结构变形,这引起DNA酶半部的分裂和过氧化物酶模拟活性的降低。因此,在AFB1的存在下,浓度依赖性在0.1-1.0 x 10(4)ng / mL范围内,比色检测极限为0.1 ng / mL,则催化过程产生的比色信号会降低。 。新的测定系统对AFB1的选择性比其他霉菌毒素高,可用于检测地面玉米样品中AFB1的存在。总体而言,该策略应作为开发快速,简单和低成本的真菌毒素检测方法的基础。 (C)2015 Elsevier B.V.保留所有权利。

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