Electrochemical biosensor based on base-stacking-dependent DNA hybridization assay for protein detection

被引:12
|
作者
Li, Hao [1 ,2 ]
Zhang, Wei [1 ]
Zhou, Honghao [1 ]
机构
[1] Cent S Univ, Inst Clin Pharmacol, Changsha 410078, Hunan, Peoples R China
[2] Hunan Prov Peoples Hosp, Dept Hepatobiliary Surg, Changsha 410002, Hunan, Peoples R China
关键词
Stacking-dependent DNA hybridization assay; Protein detection; alpha-Fetoprotein; Differential pulse voltammetry; ALPHA-FETOPROTEIN; PAIRING CONTRIBUTIONS; DOUBLE-HELIX; IMMUNOASSAY; IMMUNOSENSOR; STABILITY; AMPLIFICATION; QUANTITATION; APTASENSORS; MOLECULES;
D O I
10.1016/j.ab.2013.12.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An antibody-based electrochemical biosensing platform has been developed and used for the detection of protein. In the presence of the target, an antibody pair binds to the protein simultaneously, which causes two oligo-DNAs conjugated with the antibody pair to hybridize to each other and become a big "stem-loop" structure. Subsequently, the longer oligo-DNA of the stem, with a methylene blue (MB) label at the terminal, hybridizes stably with capture DNA owing to the enhancement of base stacking. The strong redox current signal of MB is used for protein quantification. Using alpha-fetoprotein (AFP) as a model, the proposed method could detect AFP at a concentration as low as 2 pg ml(-1) with a dynamic range of 4 orders of magnitude, which approaches traditional assays such as enzyme-linked immunosorbent assay. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:26 / 31
页数:6
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