Highly sensitive and selective optical detection of lead(II) using a label-free fluorescent aptasensor

被引:26
作者
Huang, Yafei [1 ,2 ,3 ]
Yan, Jiao [1 ,2 ,3 ]
Fang, Zongzhuang [1 ,2 ]
Zhang, Chenghui [1 ]
Bai, Wenhui [2 ,3 ]
Yan, Mengmeng [2 ,3 ]
Zhu, Chao [2 ,3 ]
Gao, Chengguo [4 ]
Chen, Ailiang [2 ,3 ]
机构
[1] Hainan Univ, Coll Food Sci & Technol, Haikou 570228, Peoples R China
[2] Chinese Acad Agr Sci, Key Lab Agroprod Qual & Safety, Inst Qual Stand & Testing Technol Agroprod, Beijing 100081, Peoples R China
[3] Minist Agr, Key Lab Agrifood Qual & Safety, Beijing 100081, Peoples R China
[4] Gansu Zeacen Yeast Technol Co Ltd, Baiyin 730900, Peoples R China
关键词
G-QUADRUPLEX; TURN-ON; METAL-IONS; BIOSENSOR; DNAZYME; PB2+; ENRICHMENT; MOLECULES; APTAMER; LIGANDS;
D O I
10.1039/c6ra15750e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lead (Pb) is a heavy metal that does great harm to human bodies through its accumulation in the food chain. It remains a challenge to use environment-friendly and biocompatible materials to sensitively detect lead in organisms and aquatic ecosystems. To achieve highly sensitive and selective Pb2+ detection, a sensor based on ultra-sensitive double-stranded DNA (dsDNA) specific dye PicoGreen and label-free oligonucleotides was reported. The principle of this method is that the Pb2+ induced a structural change of G-rich thrombin aptamer from random coil to G-quadruplex, which prevented its binding to its complementary sequences to form dsDNA and caused a fluorescence intensity decrease with PicoGreen. The results showed that this method satisfied the requirement of the maximum residue limit (MRL) of Pb2+ and could detect Pb2+ at a lowest concentration of 1 ng mL(-1) within a dynamic range of six orders of magnitude. Since the aptamer was highly specific, this method showed high Pb2+ selectivity against eight other metals. Finally, the proposed assay was successfully validated by determining Pb2+ in water samples.
引用
收藏
页码:90300 / 90304
页数:5
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