"Blue-red-purple" multicolored lateral flow immunoassay for simultaneous detection of GM crops utilizing RPA and CRISPR/Cas12a

被引:0
|
作者
Wang, Jinbin [1 ,2 ]
Luo, Jiawei [1 ,3 ]
Liu, Hua [1 ,2 ]
Xu, Danhong [1 ]
Li, You [1 ]
Liu, Xiaofeng [3 ]
Zeng, Haijuan [1 ,2 ,4 ]
机构
[1] Shanghai Acad Agr Sci, Biotechnol Res Inst, Key Lab Agr Genet & Breeding, Shanghai 201106, Peoples R China
[2] Minist Agr & Rural Affairs, Crops Ecol Environm Secur Inspect & Supervis Ctr, Key Lab Safety Assessment Environm Agr Genet Modif, Shanghai 201106, Peoples R China
[3] Lanzhou Univ Technol, Sch Life Sci & Engn, Lanzhou 730050, Peoples R China
[4] Shanghai Coelite Agr Sci Tech Grp Co Ltd, Shanghai 201106, Peoples R China
关键词
Multicolored lateral flow immunoassay; Simultaneous detection; RPA; CRISPR/Cas12a; GM crops;
D O I
10.1016/j.talanta.2024.127010
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Advanced multiplexed testing techniques should be designed and developed to ensure an accurate and reliable evaluation for unknown samples. In this study, an efficient platform coupled with the "Blue-Red-Purple" strategy based on recombinant polymerase amplification (RPA), CRISPR/Cas12a and lateral flow strip was established, which could realize the dual-target detection of CP4-EPSPS and Cry1Ab/Ac in genetically modified crops. The lateral flow immunoassay was developed using different colored microspheres to label the antibodies to realize the visualization of results and avoid cross-reactions. The proposed method exhibits high specificity, sensitivity and stability. The visual detection limits of standard plasmids and real samples reached 10 copies/mu L and 0.5 %, respectively, which could be stored at 4 degrees C for 12 months with high detection ability. Moreover, the entire detection process could be completed within 50 min without any complex instruments or professional operators. These findings indicated that a sensitive, specific, rapid and accurate method was established for on-site detection of GM crops.
引用
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页数:9
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