Ultrasensitive Detection of Pb2+ Based on a DNAzyme and Digital PCR
In this study, an ultrasensitive detection method for aqueous Pb2+ based on digital polymerase chain reaction (dPCR) technology and a Pb2+-dependent DNAzyme was developed. In the presence of Pb2+, the Gr-5 DNAzyme was activated and catalyzed the hydrolytic cleavage of the substrate strand, resulting...
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doaj-03949cf0ce384082acb60e3d655a0d692020-11-25T00:35:44ZengHindawi LimitedJournal of Analytical Methods in Chemistry2090-88652090-88732019-01-01201910.1155/2019/35283453528345Ultrasensitive Detection of Pb2+ Based on a DNAzyme and Digital PCRTao Zhang0Cong Liu1Wuping Zhou2Keming Jiang3Chenyu Yin4Cong Liu5Zhiqiang Zhang6Haiwen Li7Key Lab of Bio-Medical Diagnostics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou 215163, ChinaKey Lab of Bio-Medical Diagnostics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou 215163, ChinaKey Lab of Bio-Medical Diagnostics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou 215163, ChinaKey Lab of Bio-Medical Diagnostics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou 215163, ChinaKey Lab of Bio-Medical Diagnostics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou 215163, ChinaKey Lab of Bio-Medical Diagnostics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou 215163, ChinaKey Lab of Bio-Medical Diagnostics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou 215163, ChinaKey Lab of Bio-Medical Diagnostics, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou 215163, ChinaIn this study, an ultrasensitive detection method for aqueous Pb2+ based on digital polymerase chain reaction (dPCR) technology and a Pb2+-dependent DNAzyme was developed. In the presence of Pb2+, the Gr-5 DNAzyme was activated and catalyzed the hydrolytic cleavage of the substrate strand, resulting in an increase in the amount of template DNA available for dPCR and a resultant change in the number of droplets showing a positive signal. Moreover, the detection system was found to be sensitive and stable in environmental sample detection. In summary, an ultrasensitive quantitative detection method for Pb2+ within environmental substrates was established.http://dx.doi.org/10.1155/2019/3528345 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tao Zhang Cong Liu Wuping Zhou Keming Jiang Chenyu Yin Cong Liu Zhiqiang Zhang Haiwen Li |
spellingShingle |
Tao Zhang Cong Liu Wuping Zhou Keming Jiang Chenyu Yin Cong Liu Zhiqiang Zhang Haiwen Li Ultrasensitive Detection of Pb2+ Based on a DNAzyme and Digital PCR Journal of Analytical Methods in Chemistry |
author_facet |
Tao Zhang Cong Liu Wuping Zhou Keming Jiang Chenyu Yin Cong Liu Zhiqiang Zhang Haiwen Li |
author_sort |
Tao Zhang |
title |
Ultrasensitive Detection of Pb2+ Based on a DNAzyme and Digital PCR |
title_short |
Ultrasensitive Detection of Pb2+ Based on a DNAzyme and Digital PCR |
title_full |
Ultrasensitive Detection of Pb2+ Based on a DNAzyme and Digital PCR |
title_fullStr |
Ultrasensitive Detection of Pb2+ Based on a DNAzyme and Digital PCR |
title_full_unstemmed |
Ultrasensitive Detection of Pb2+ Based on a DNAzyme and Digital PCR |
title_sort |
ultrasensitive detection of pb2+ based on a dnazyme and digital pcr |
publisher |
Hindawi Limited |
series |
Journal of Analytical Methods in Chemistry |
issn |
2090-8865 2090-8873 |
publishDate |
2019-01-01 |
description |
In this study, an ultrasensitive detection method for aqueous Pb2+ based on digital polymerase chain reaction (dPCR) technology and a Pb2+-dependent DNAzyme was developed. In the presence of Pb2+, the Gr-5 DNAzyme was activated and catalyzed the hydrolytic cleavage of the substrate strand, resulting in an increase in the amount of template DNA available for dPCR and a resultant change in the number of droplets showing a positive signal. Moreover, the detection system was found to be sensitive and stable in environmental sample detection. In summary, an ultrasensitive quantitative detection method for Pb2+ within environmental substrates was established. |
url |
http://dx.doi.org/10.1155/2019/3528345 |
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