An enzyme-amplified lateral flow strip biosensor for visual detection of MicroRNA-224

被引:75
作者
Gao, Xuefei [1 ]
Xu, Li-Ping [1 ]
Wu, Tingting [1 ]
Wen, Yongqiang [1 ]
Ma, Xinlei [1 ]
Zhang, Xueji [1 ]
机构
[1] Univ Sci & Technol Beijing, Res Ctr Bioengn & Sensing Technol, Beijing 100083, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
MicroRNA; Lateral flow biosensor; Visual detection; Signal amplification; Horseradish peroxidase; EXPRESSION; SINGLE; PROBE; MIRNA; PCR;
D O I
10.1016/j.talanta.2015.06.060
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An enzyme-based dual-labeled nanoprobe is designed to fabricate a sensitive enzyme-amplified lateral flow biosensor for visual detection of mircoRNA-224 (miRNA-224). The recognition DNA probe (detection probe) and signal amplification enzyme (Horseradish peroxidase, HRP) are immobilized on gold nano-particle (GNPs) surface, simultaneously. The capture DNA probes are immobilized on the test zone of the lateral flow biosensor. When miRNA-224 is present, the enzyme-based dual-labeled nanoprobes will be captured by forming the "sandwich structure" on the test zone of the lateral flow biosensor, enabling the visual detection for miRNA-224. Sensitivity is amplified by applying the 3,3,5,5-tetramethylbenzidine enzymatic substrate (TMB/H2O2 enzymatic substrate) onto the test zone. The enzymatic reactions between the HRP and the TMB/H2O2 enzymatic substrate will produce blue products, which deposit on the nanoprobe surface to enhance the visual effect and the corresponding response intensities of the test zone. This enzyme-amplified lateral flow biosensor shows a low limit of detection (LOD) (7.5 pM) toward miRNA-224 in the buffer solution, which is improved by 10-fold than that of the single-labeled lateral flow biosensor. This biosensor has been successfully used for the detection of the target miRNA-224 detection in A549 cell lysate. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:648 / 654
页数:7
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