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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 >Low-cost and highly efficient DNA biosensor for heavy metal ion using specific DNAzyme-modified microplate and portable glucometer-based detection mode
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Low-cost and highly efficient DNA biosensor for heavy metal ion using specific DNAzyme-modified microplate and portable glucometer-based detection mode

机译:使用特定的DNAzyme修饰微孔板和基于便携式血糖仪的检测模式,低成本,高效的重金属离子DNA生物传感器

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摘要

A simple and low-cost DNA sensing platform based on Pb2+-specific DNAzyme-modified microplate was successfully developed for highly sensitive monitoring of lead ion (Pb2+, one kind of toxic heavy metal ion) in the environmental samples coupling with a portable personal glucometer (PGM)-based detection mode. The detection cell was first prepared simply by means of immobilizing the DNAzyme on the streptavidin-modified microplate. Gold nanoparticle labeled with single-stranded DNA and invertase (Enz-AuNP-DNA) was utilized as the signal-transduction tag to produce PGM substrate (glucose). Upon addition of lead ion into the microplate, the substrate strand of the immobilized DNAzyme was catalytically cleaved by target Pb2+, and the newly generated single-strand DNA in the microplate could hybridize again with the single-stranded DNA on the Enz-AuNP-DNA. Accompanying with the Enz-AuNP-DNA, the carried invertase could convert sucrose into glucose. The as-produced glucose could be monitored by using a widely accessible PGM for in situ amplified digital readout. Based on Enz-AuNP-DNA amplification strategy, as low as 1.0 pM Pb2+ could be detected under the optimal conditions. Moreover, the methodology also showed good reproducibility and high selectivity toward target Pb2+ against other metal ions because of highly specific Pb2+-dependent DNAzyme, and was applicable for monitoring Pb2+ in the naturally contaminated sewage and spiked drinking water samples. (C) 2015 Elsevier B.V. All rights reserved.
机译:成功开发了一种基于Pb2 +特异性DNAzyme修饰微孔板的简单,低成本的DNA传感平台,可与便携式个人血糖仪(结合使用)高度灵敏地监测环境样品中的铅离子(Pb2 +,一种有毒的重金属离子)。基于PGM)的检测模式。首先简单地通过将DNA核酶固定在链霉亲和素修饰的微板上来制备检测细胞。利用单链DNA和转化酶标记的金纳米颗粒(Enz-AuNP-DNA)作为信号转导标签产生PGM底物(葡萄糖)。向微孔板中添加铅离子后,固定的DNAzyme的底物链被目标Pb2 +催化切割,并且微孔板中新生成的单链DNA可以再次与Enz-AuNP-DNA上的单链DNA杂交。 。携带的转化酶与Enz-AuNP-DNA一起可以将蔗糖转化为葡萄糖。产生的葡萄糖可通过使用广泛使用的PGM进行原位扩增数字读数进行监测。基于Enz-AuNP-DNA扩增策略,在最佳条件下可检测到低至1.0 pM Pb2 +。此外,该方法由于对Pb2 +的依赖度很高,因此对其他金属离子的目标Pb2 +具有良好的重现性和高选择性,可用于监测自然污染的污水和加标饮用水样品中的Pb2 +。 (C)2015 Elsevier B.V.保留所有权利。

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