Label-free fluorescent strategy for sensitive detection of tetracycline based on triple-helix molecular switch and G-quadruplex

被引:1
|
作者
Tian-Xiao Chen [1 ]
Feng Ning [2 ]
Hai-Sheng Liu [2 ]
Ke-Feng Wu [2 ]
Wei Li [1 ]
Chang-Bei Ma [2 ]
机构
[1] School of Chemistry and Biological Engineering, Changsha University of Science and Technology
[2] State Key Laboratory of Medical Genetics & School of Life Sciences, Central South University
基金
中国国家自然科学基金;
关键词
Tetracycline; Aptamer; Label-free; Triple-helix molecular switch; G-quadruplex; Thioflavin T;
D O I
暂无
中图分类号
O657.3 [光化学分析法(光谱分析法)]; TS207.5 [食品污染度的测定];
学科分类号
070302 ; 081704 ; 083201 ;
摘要
In this assay, a label-free fluorescent sensing platform based on triple-helix molecular switch(THMS) and G-quadruplex was developed for the detection of tetracycline. We demonstrated this approach by using THMS, which consists of a central section with a shortened 8-mer aptamer sequence with high affinity to tetracycline and flanked by two arm segments. G-rich oligonucleotide can specifically bind to thioflavin T(Th T) as a signal transduction probe(STP). In the absence of tetracycline, THMS remains stable, the fluorescence of background is low. By the addition of target tetracycline, the aptamer-target binding results in the formation of a structured aptamer-target complex, which disassembles the THMS and releases the STP. The free STP self-assembles into G-quadruplex and specifically binds to Th T which generates a obvious fluorescence enhancement. Using the triple-helix molecular switch, the developed aptamer-based fluorescent sensing platform showed a linear relationship with the concentration of tetracycline ranging from 0.2 to 20.0 nmol/L. The detection limit of tetracycline was determined to be970.0 pmol/L. The assay avoids complicated modifications or chemical labeling, making it simple and cost-effective. So, it is expected that this aptamer-based fluorescent assay could be extensively applied in the field of food safety inspection.
引用
收藏
页码:1380 / 1384
页数:5
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