A homogeneous hemin/G-quadruplex DNAzyme based turn-on chemiluminescence aptasensor for interferon-gamma detection via in-situ assembly of luminol functionalized gold nanoparticles, deoxyribonucleic acid, interferon-gamma and hemin

被引:41
作者
Jiang, Jie [1 ]
He, Yi [1 ]
Yu, Xiuxia [1 ]
Zhao, Jinyang [1 ]
Cui, Hua [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, CAS Key Lab Soft Matter Chem, Hefei 230026, Anhui, Peoples R China
关键词
Chemiluminescence; Luminol functionalized gold nanoparticles; Aptasensor; Homogeneous; Interferon-gamma; DNAzyme; LABEL-FREE; ELECTROCHEMICAL DETECTION; HORSERADISH-PEROXIDASE; DNA DETECTION; APTAMER; ELECTROCHEMILUMINESCENCE; PLATFORM; SIGNAL; BLOOD; FLUORESCENCE;
D O I
10.1016/j.aca.2013.06.048
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A homogeneous hemin/G-quadruplex DNAzyme (HGDNAzyme) based turn-on chemiluminescence aptasensor for interferon-gamma (IFN-gamma) detection is developed, via dynamic in-situ assembly ofluminol functionalized gold nanoparticles (lum-AuNPs), DNA, IFN-gamma and hemin. The G-quadruplex oligomer of the HGDNAzyme was split into two halves, which was connected with the complementary sequence of P1 (IFN-gamma-binding aptamer) to form the oligonucleotide P2. P2 hybridized with IFN-gamma-binding aptamer and meanwhile assembled onto lum-AuNPs through biotin-streptavidin specific interaction. When IFN-gamma was recognized by aptamer, P2 was released into the solution. The two lateral portions of P2 combined with hemin to yield the catalytic hemin/G-quadruplex DNAzyme, which amplified the luminol oxidation for a turn-on chemiluminescence signaling. Based on this strategy, the homogeneous aptasensor enables the facile detection of IFN-gamma in a range of 0.5-100 nM. Moreover, the aptasensor showed high sensitivity (0.4 nM) and satisfactory specificity, pointing to great potential applications in clinical analysis. (C) 2013 Published by Elsevier B.V.
引用
收藏
页码:60 / 64
页数:5
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