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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 >Enzyme-free and label-free ultra-sensitive colorimetric detection of Pb2+ using molecular beacon and DNAzyme based amplification strategy
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Enzyme-free and label-free ultra-sensitive colorimetric detection of Pb2+ using molecular beacon and DNAzyme based amplification strategy

机译:使用分子信标和基于DNAzyme的扩增策略对Pb2 +进行无酶和无标记的超灵敏比色检测

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摘要

An enzyme-free and label-free colorimetric Pb2+ sensor based on DNAzyme and molecular beacon (MB) has been developed and demonstrated by recycle using enzyme strand for signal amplification. The substrate strand DNA (S-DNA) of DNAzyme could be converted into MB structure with base pairs of stem part at the both ends. The MB could hybridize with enzyme strand DNA (E-DNA) to form DNAzyme, and be activated and cleaved in the presence of Pb2+. The cleaved MB is much less stable, releasing from the DNAzyme as two product pieces. The product pieces of MB are flexible and could bind to unmodified AuNPs to effectively stabilize them against salt-induced aggregation. Then, the E-DNA is liberated to catalyze the next reaction and amplify the response signal. By taking advantage of repeated using of E-DNA, our proposed method exhibited high sensitive for Pb2+ detection in a linear range from 0.05 to 5 nM with detection limit of 20 pM by UV-vis spectrometer. Moreover, this method was also used for determination of Pb2+ in river water samples with satisfying results. Importantly, this strategy could reach high sensitivity without any modification and complex enzymatic or hairpins based amplification procedures. (C) 2016 Elsevier B.V. All rights reserved.
机译:已开发出一种基于DNAzyme和分子信标(MB)的无酶,无标签的比色Pb2 +传感器,并已通过使用酶链进行信号放大的循环利用加以证明。 DNAzyme的底物链DNA(S-DNA)可以转化为MB结构,两端具有茎部碱基对。 MB可以与酶链DNA(E-DNA)杂交形成DNAzyme,并在Pb2 +存在下被激活和切割。裂解的MB不稳定得多,以两个产物片段的形式从DNAzyme释放。 MB的产品片段具有柔韧性,可以与未修饰的AuNP结合,从而有效地稳定它们免受盐诱导的聚集。然后,释放E-DNA以催化下一个反应并放大反应信号。利用重复使用E-DNA的优势,我们提出的方法对Pb2 +的检测具有很高的灵敏度,线性范围为0.05到5 nM,UV-vis光谱仪的检测极限为20 pM。此外,该方法还用于测定河水样品中的Pb2 +,结果令人满意。重要的是,该策略无需进行任何修饰和复杂的基于酶或发夹的扩增程序即可达到高灵敏度。 (C)2016 Elsevier B.V.保留所有权利。

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