Signal amplification for DNA detection based on the HRP-functionalized Fe3O4 nanoparticles

被引:32
作者
Dong, Xiao-Ya [1 ]
Mi, Xiao-Na [1 ]
Wang, Bo [1 ]
Xu, Jing-Juan [1 ]
Chen, Hong-Yuan [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Key Lab Analyt Chem Life Sci, MOE, Nanjing 210093, Peoples R China
关键词
Electrochemical sensor; Gold nanofilm; Bioconjugates; DNA biosensors; AMPLIFIED ELECTROCHEMICAL IMMUNOASSAY; CARBON-NANOTUBES; MACROPOROUS GOLD; BIOSENSOR; FILM; DEPOSITION; ELECTRODE; PROTEINS; LABEL; OXIDE;
D O I
10.1016/j.talanta.2011.01.060
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An electrochemical approach for the sensitive detection of sequence-specific DNA has been developed. Horseradish peroxidase (HRP) assembled on the Fe3O4 nanoparticles (NPs) were utilized as signal amplification sources. High-content HRP was adsorbed on the Fe3O4 NPs via layer-by-layer (LbL) technique to prepare HRP-functionalized Fe3O4 NPs. Signal probe and diluting probe were then immobilized on the HRP-functionalized Fe3O4 NPs through the bridge of Au NPs. Thereafter, the resulting DNA-Au-HRP-Fe3O4 (DAHF) bioconjugates were successfully anchored to the gold nanofilm (GNF) modified electrode surface for the construction of sandwich-type electrochemical DNA biosensor. The electrochemical behaviors of the prepared biosensor had been investigated by the cyclic voltammetry (CV), chronoamperometry (i-t), and electrochemical impedance spectroscopy (EIS). Under optimal conditions, the proposed strategy could detect the target DNA down to the level of 0.7 fmol with a dynamic range spanning 4 orders of magnitude and exhibited excellent discrimination to two-base mismatched DNA and non-complementary DNA sequences. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:531 / 537
页数:7
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