A label-free DNAzyme fluorescence biosensor for amplified detection of Pb2+-based on cleavage-induced G-quadruplex formation

被引:50
|
作者
Fu, Ting [1 ]
Ren, Songlei [1 ]
Gong, Liang [1 ]
Meng, Hongmin [1 ]
Cui, Liang [1 ]
Kong, Rong-Mei [2 ]
Zhang, Xiao-Bing [1 ]
Tan, Weihong [1 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
[2] Qufu Normal Univ, Coll Chem & Chem Engn, Key Lab Life Organ Anal, Qufu 273165, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
DNAzyme; label-free; G-quadruplex; Biosensor; Fluorescence; CATALYTIC BEACON SENSOR; HIGH-SENSITIVITY; METAL-IONS; LEAD; DNA; SELECTIVITY; PROBE; SPECTROMETRY; VOLTAMMETRY; CHEMISTRY;
D O I
10.1016/j.talanta.2015.10.004
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
DNAzyme-based catalytic beacons have been widely studied for both in vivo and in vitro molecular detection. However, only a few label-free catalytic beacons with excellent analytical performance have been reported so far. In this work, by combining a catalytic DNAzyme for amplified sensing through enzymatic turnover with cleavage-induced G-quadruplex formation, a label-free DNAzyme biosensor was developed for amplified "turn-on" fluorescence detection of Pb2+ with a detection limit of 3 nM. The method is very competitive compared to many other labeled or label-free methods with or without signal amplification. Due to the inherent specificity of the GR-5 DNAzyme, the method also exhibits excellent selectivity. This biosensor successfully detected Pb2+ in river water samples with high sensitivity and selectivity. Such a method might provide a universal DNAzyme-based sensing platform for sensitive detection of various targets both in environmental and biomedical fields. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:302 / 306
页数:5
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