Fluorescent aptasensor for detection of four tetracycline veterinary drugs in milk based on catalytic hairpin assembly reaction and displacement of G-quadruplex

被引:29
作者
Zhou, Chen [1 ]
Zou, Haimin [1 ,2 ]
Sun, Chengjun [1 ]
Ren, Dongxia [1 ]
Xiong, Wei [1 ]
Li, Yongxin [1 ,3 ]
机构
[1] Sichuan Univ, West China Sch Publ Hlth, 17 South Renmin Rd, Chengdu 610041, Sichuan, Peoples R China
[2] Chengdu Ctr Dis Control & Prevent, Chengdu 610031, Sichuan, Peoples R China
[3] Sichuan Univ, Coll Life Sci, 29 Wangjiang Rd, Chengdu 610064, Sichuan, Peoples R China
基金
中国博士后科学基金;
关键词
Tetracycline veterinary drugs; Milk samples; Fluorescence; G-quadruplex; N-methylmesoporphyrin IX; Catalytic hairpin assembly; TANDEM MASS-SPECTROMETRY; PERFORMANCE LIQUID-CHROMATOGRAPHY; ASSAY-BASED APTASENSOR; ANTIBIOTIC-RESIDUES; COLORIMETRIC DETECTION; TRACE TETRACYCLINE; IONIC LIQUID; APTAMER; HONEY; DNA;
D O I
10.1007/s00216-018-0981-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Based on a novel signal amplification strategy by catalytic hairpin assembly and displacement of G-quadruplex DNA, an enzyme-free, non-label fluorescent aptasensing approach was established for sensitive detection of four tetracycline veterinary drugs in milk. The network consisted of a pair of partially complementary DNA hairpins (HP1 and HP2). The DNA aptamer of four tetracycline veterinary drugs was located at the sticky end of the HP1. The ring region of HP1 rich in G and C could form a stable G-quadruplex structure, which could emit specific fluorescence signal after binding with the fluorescent dye and N-methylmesoporphyrin IX (NMM). When presented in the system, the target analytes would be repeatedly used to trigger a recycling procedure between the hairpins, generating numerous HP1-HP2 duplex complexes and displacing G-quadruplex DNA. Thus, the sensitive detection of target analytes was achieved in a wide linear range (0-1000 mu g/L) with the detection limit of 4.6 mu g/L. Moreover, this proposed method showed high discrimination efficiency towards target analytes against other common mismatched veterinary drugs, and could be successfully applied to the analysis of milk samples.
引用
收藏
页码:2981 / 2989
页数:9
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