Ultrasensitive electrochemical biosensor for protein detection based on target-triggering cascade enzyme-free signal amplification strategy

被引:6
作者
Ling, Pinghua [1 ]
Wang, Linyu [1 ]
Cheng, Shan [1 ]
Gao, Xianping [1 ]
Sun, Xinyu [1 ]
Gao, Feng [1 ]
机构
[1] Anhui Normal Univ, Coll Chem & Mat Sci, Anhui Key Lab Chemo Biosensing, Minist Educ,Lab Functionalized Mol Solids, Wuhu 241002, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemical biosensor; Thrombin; Enzyme-free; Signal amplification; DETECTION PLATFORM; LABEL-FREE; THROMBIN; APTASENSOR; APTAMER; ASSAY; DNAZYME; BIND; BIORECOGNITION; NANOCOMPOSITE;
D O I
10.1016/j.aca.2022.339675
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein, a cost-effective, simple and sensitive electrochemical sensing platform was established based on aptamer target recognition and target-triggering signal amplification strategy for protein detection. Due to the high affinity between the aptamer and target, the assistant DNA1 (a1) could release from a1aptamer duplex and trigger the following DNA circuits. The strand displacement and branch migration reaction brought assistant DNA3 (a3) released. Eventually, a large number of duplex structures of a3 -Hairpin DNA3 were formed on the surface of electrode. Consequently, the capture DNA on the surface of platinum nanoparticles could hybridize with the unfolded DNA fragment of Hairpin DNA3 on the sensor surface, resulting in the electrochemical signal readout of H2O2 reduction. Using thrombin as a model target, under the optimal conditions, this method exhibited a linear detection range from 0.5 pM to 300 nM with a detection limit of 0.17 pM. The proposed detection strategy was enzyme-free and exhibited good selectivity and sensitivity for a variety of protein targets detection by using corresponding DNA-based affinity probes, which makes it possible to apply the sensor for sensitivity detection of analytes in bioassays.(c) 2022 Published by Elsevier B.V.
引用
收藏
页数:6
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