An ultrasensitive chemiluminescent immunosensor for the detection of human leptin using hemin/G-quadruplex DNAzymes-assembled signal amplifier

被引:25
|
作者
He, Yuezhen [1 ]
Wang, Xiaoxun [1 ]
Zhang, Yuzhong [1 ]
Gao, Feng [1 ]
Li, Yongxin [1 ]
Chen, Hongqi [1 ]
Wang, Lun [1 ]
机构
[1] Anhui Normal Univ, Anhui Key Lab Chemobiosensing, Key Lab Funct Mol Solids, Minist Educ,Coll Chem & Mat Sci, Wuhu 241000, Peoples R China
关键词
Chemiluminescent immunoassay; Human leptin; Hemin; G-quadruplex; DNAzymes; Horseradish peroxidase; RESONANCE ENERGY-TRANSFER; LUMINOL; DNA; IMMUNOASSAY; EXPRESSION; APTASENSOR; GRAPHENE;
D O I
10.1016/j.talanta.2013.07.074
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, we reported a sensitive chemiluminescent immunosensor for the detection of human leptin by using hemin/G-quadruplex DNAzymes to amplify detection signal. In this sensing system, the primary antibody (anti-human leptin) was firstly bound to the 96-well plates, and human leptin and biotinylated secondary antibody were successively combined to form sandwich-type immune complex through specific interactions. Then streptavidin labeled with hemin/G-quadruplex DNAzymes was assembled to the sandwich-type immunocomplex by streptavidin-biotin interaction. The DNAzymes exhibited an excellent catalytic activity to the chemiluminescent reaction of luminol with hydrogen peroxide in strong alkaline solution, leading to significant enhancement in response signal. Under the optimum conditions, the proposed immunosensor showed high sensitivity and selectivity with a low detection limit of 1.9 pg mL(-1) and a wide linear response range of human leptin from 10 to 1000 pg mL-1. The immunosensor was used to detect human leptin in serum, and the results were in good agreement with the data obtained by conventional ELISA method. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:816 / 821
页数:6
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