Target-assistant Zn2+-dependent DNAzyme for signal-on electrochemiluminescent biosensing

被引:20
作者
Huang, Yin [1 ]
Lei, Jianping [1 ]
Cheng, Yan [1 ]
Ju, Huangxian [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemiluminescence; Quantum dots; DNAzyme; Electrocatalysis; Biosensing; RESONANCE ENERGY-TRANSFER; ELECTROGENERATED CHEMILUMINESCENCE; QUANTUM DOTS; GOLD NANOPARTICLES; MOLECULAR BEACON; GRAPHENE; ATP; IMMUNOASSAY; LUMINOL; SYSTEM;
D O I
10.1016/j.electacta.2014.12.165
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A signal-on electrochemiluminescent (ECL) approach for ultrasensitive ATP detection was developed using target-assistant Zn2+-dependent DNAzyme via a dual quenching pathway between quantum dots (QDs) and Au nanoclusters (Au NCs). The facile ECL biosensor was constructed by covalent assembly of Au NCs-labeled hairpin DNA on QDs modified glassy carbon electrode. A dual quenching ECL mechanism was identified to be via resonance energy transfer between QDs and Au NCs and electrocatalytic reduction of coreactant oxygen by Au NCs. With the assistance of two help DNAs, the G-quadruplex structure of ATP aptamer was formed, and thus narrowed the two fragments of Zn2+-dependent DNAzyme. In the presence of Zn2+, Zn2+-dependent DNAzyme can be generated in situ on the biosensor's surface. The as-prepared DNAzyme can cleave the substrate strand, and release the Au NCs from the electrode, resulting in the signal-on ECL state. This biosensor showed good analytical performance with 4 orders magnitude linear range, excellent specificity, and acceptable stability. The biosensor had been applied in detection of ATP in real serum sample and provided significant potential application in clinical analysis. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:341 / 347
页数:7
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