A novel amplification strategy based on target-induced multicomponent nuclease-mediated catalytic hairpin assembly for fluorescent DNA sensor

被引:0
|
作者
Xu, Hongyan [1 ]
Xiao, Chengui [2 ]
Zhao, Fengjuan [2 ]
Suo, Zhiguang [1 ]
Liu, Yong [3 ]
Wei, Min [1 ]
Jin, Baohui [2 ]
机构
[1] Henan Univ Technol, Coll Food Sci & Technol, Henan Key Lab Cereal & Oil Food Safety & Nutr, Zhengzhou 450001, Peoples R China
[2] Shenzhen Acad Inspection & Quarantine, Food Inspect & Quarantine Technol Ctr Shenzhen Cus, Shenzhen 518045, Peoples R China
[3] Henan Univ, Sch Energy Sci & Technol, Kaifeng 475004, Peoples R China
关键词
Fluorescent biosensing; MNAzyme; Catalytic hairpin assembly; Cascade amplification; OCHRATOXIN;
D O I
10.1016/j.saa.2025.125979
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Ochratoxin A (OTA) is a highly hazardous mycotoxin widely found in food ingredients and processed products. In response to the demand for food safety, there is an urgent need to establish a highly sensitive, reliable, and costeffective method for the detection of OTA. In this study, a simple, enzyme-free, sensitive cascade amplification fluorescent strategy was developed to detect OTA based on a magnetic separation system-assisted, multicomponent nuclease (MNAzyme) and its induced catalytic hairpin assembly (CHA). The formation of a stable active MNAzyme was induced by the presence of the target, and the MNAzyme specifically cleaved multiple hairpin H1 to produce sDNA fragments. The sDNA could initiate the mismatched CHA cycle, leading to the production of a large number of H2-H3 complexes, with carboxyfluorescein (FAM) moving away from the quench group (BHQ1), and the fluorescent signal being significantly amplified. The constructed fluorescent aptasensor has a good linear range (0.5-100 ng/mL) and detection limit (0.45 ng/mL). The developed sensor was successfully applied to detect OTA in corn flour and black tea samples.
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页数:10
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