CRISPR/Cas12a-Assisted Chemiluminescence Sensor for Aflatoxin B1 Detection in Cereal Based on Functional Nucleic Acid and In-Pipet Rolling Circle Amplification

被引:30
作者
Wang, Zhilong [1 ]
Wei, Luyu [1 ]
Ruan, Shilong [2 ]
Chen, Yiping [1 ,3 ,4 ]
机构
[1] Huazhong Agr Univ, Coll Food Sci & Technol, Wuhan 430070, Hubei, Peoples R China
[2] Daye Publ Inspection & Test Ctr, Daye 435100, Hubei, Peoples R China
[3] Guangdong Lab Lingnan Modern Agr, Guangzhou 510642, Guangdong, Peoples R China
[4] Chinese Acad Agr Sci, Agr Genom Inst Shenzhen, Shenzhen Branch, Guangdong Lab Lingnan Modern Agr,Genome Anal Lab M, Shenzhen 518120, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
mycotoxin; CRISPR; Cas system; aptamer; horseradish peroxidase; versatile signal reporter; CRISPR-CAS12A; CHROMATOGRAPHY; APTASENSOR; ASSAY;
D O I
10.1021/acs.jafc.3c00341
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Herein, we report a CRISPR/Cas12a-assisted chemiluminescence sensor for aflatoxin B1 (AFB1) detection based on functional nucleic-acid-mediated target recognition and in-pipet rolling circle amplification-mediated signal amplification. In this sensor, we performed rolling circle amplification on the inside of the pipet to enrich horseradish peroxidase (pipet-poly-HRP). When AFB1 is present, it interacts with functional nucleic acids and results in the release of the activator. The activator is designed to activate the CRISPR/Cas12a system, which cleaves the pipet-poly-HRP to liberate HRP. The freed HRP can then be measured by chemiluminescence to quantify AFB1. This CRISPR/Cas12a-assisted chemiluminescence sensor enables facile, highly sensitive, and specific detection of AFB1 , with a linear range from 50 pg/mL to 100 ng/mL and a detection limit of 5.2 pg/mL. Furthermore, it exhibits satisfactory recovery and has successfully challenged AFB1 detection in cereal samples. The proposed sensor offers a novel rapid screening approach that holds great promise for food security monitoring.
引用
收藏
页码:4417 / 4425
页数:9
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