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A new enzyme-free and ultrasensitive electrochemical Pb2+ biosensor was developed. By coupling the DNA-assisted cascade of hybridization reaction with the quantum dots (QDs) for signal amplification, a detection limit as low as 6.1 pM can be obtained for Pb2+. In this study, the "8-17" DNAzyme was used for specific recognition of Pb2+. In the presence of Pb2+, the DNAzyme was activated and cleaved the substrate strand. And then, the hybridization between the linker probe and signal probe was initiated, which resulted in formation of a long cascade DNA structure as well as assemble of numerous QDs at last. By the use of magnetic beads, the free signal probe can be easily removed by external magnetic field. After acid lysis, a great amount of redox cations can be released from the QDs and eventually result in significantly amplified electrochemical signals. This method is highly sensitive, selective and simple without the participation of any protein based enzyme (nuclease), thereby holds great potential for real sample analysis. (C) 2014 Elsevier Ltd. All rights reserved.
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ELECTROCHIMICA ACTA
ISSN: 0013-4686
Year: 2014
Volume: 134
Page: 1-7
4 . 5 0 4
JCR@2014
5 . 5 0 0
JCR@2023
ESI Discipline: CHEMISTRY;
ESI HC Threshold:268
JCR Journal Grade:1
CAS Journal Grade:1
Cited Count:
WoS CC Cited Count: 37
SCOPUS Cited Count: 35
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 3