A self-assemble aptamer fragment/target complex based high-throughput colorimetric aptasensor using enzyme linked aptamer assay

被引:36
作者
Nie, Ji [1 ]
Deng, Yan [1 ]
Deng, Qin-Pei [1 ]
Zhang, De-Wen [1 ]
Zhou, Ying-Lin [1 ]
Zhang, Xin-Xiang [1 ]
机构
[1] Peking Univ, Coll Chem, Key Lab Biochem & Mol Engn, BNLMS, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
Enzyme linked aptamer assay; Colorimetry; Cocaine; Small molecule; Biomacromolecule; GOLD NANOPARTICLES; ELECTROCHEMICAL APTASENSOR; FLUORESCENCE ANISOTROPY; COCAINE; DNA; THROMBIN; DNAZYME; SENSOR; AMPLIFICATION; MOLECULES;
D O I
10.1016/j.talanta.2012.11.018
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Enzyme linked aptamer assay (ELAA) uses an aptamer as recognition element and enzyme as signal readout element for establishing different kinds of aptasensors. We reported herein a high-throughput colorimetric aptasensor based on ELAA only requiring a single aptamer sequence for cocaine detection. An anti-cocaine aptamer was cleaved into two fragments, one of which was immobilized on a DNA-BIND 96-well plate via 5'-labeled primary amine and the other one was biotin labeled. The presence of two aptamer fragments and the target molecule led to the formation of aptamer fragments/target complexes. Streptavidin-horseradish peroxidase (SA-HRP) was used to react with biotin in order to obtain quantitative signals. A linear response towards cocaine concentration in the range of 5-200 mu M and a detection limit down to 2.8 mu M (S/N=3) were achieved. The specificity and application in real sample were validated. Furthermore, a verification test of thrombin detection in the same strategy illustrated its feasibility for not only small molecule but also biomacromolecule. With the advantage of high-throughput, easy operation, high specificity, the colorimetric assay based on ELAA requiring a single aptamer sequence opens up a new approach for detecting different kinds of targets via specific affinity recognition among target and suitably cleaved aptamer fragments. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:309 / 314
页数:6
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