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利用 RPA-CRISPR/Cas12a-G4 比色分析,通过高精度深度学习目标识别和分类,快速、便携、灵敏地检测 CaMV35S。

Rapid, portable, and sensitive detection of CaMV35S by RPA-CRISPR/Cas12a-G4 colorimetric assays with high accuracy deep learning object recognition and classification.

机构信息

Key Laboratory for Biological Science and Technology of Ministry of Education, Bioengineering College of Chongqing University, Chongqing 400044, PR China.

Key Laboratory for Biological Science and Technology of Ministry of Education, Bioengineering College of Chongqing University, Chongqing 400044, PR China; Chongqing Engineering and Technology Research Center of Intelligent Rehabilitation and Eldercare, Chongqing City Management College, Chongqing, 401331, PR China.

出版信息

Talanta. 2024 Oct 1;278:126441. doi: 10.1016/j.talanta.2024.126441. Epub 2024 Jun 20.

DOI:10.1016/j.talanta.2024.126441
PMID:38924982
Abstract

Fast, sensitive, and portable detection of genetic modification contributes to agricultural security and food safety. Here, we developed RPA-CRISPR/Cas12a-G-quadruplex colorimetric assays that can combine with intelligent recognition by deep learning algorithms to achieve sensitive, rapid, and portable detection of the CaMV35S promoter. When the crRNA-Cas12a complex recognizes the RPA amplification product, Cas12 cleaves the G-quadruplex, causing the G4-Hemin complex to lose its peroxide mimetic enzyme function and be unable to catalyze the conversion of ABTS to ABTS, allowing CaMV35S concentration to be determined based on ABTS absorbance. By utilizing the RPA-CRISPR/Cas12a-G4 assay, we achieved a CaMV35S limit of detection down to 10 aM and a 0.01 % genetic modification sample in 45 min. Deep learning algorithms are designed for highly accurate classification of color results. Yolov5 objective finding and Resnet classification algorithms have been trained to identify trace (0.01 %) CaMV35S more accurately than naked eye colorimetry. We also coupled deep learning algorithms with a smartphone app to achieve portable and rapid photo identification. Overall, our findings enable low cost ($0.43), high accuracy, and intelligent detection of the CaMV35S promoter.

摘要

快速、灵敏、便携的基因修饰检测有助于农业安全和食品安全。在这里,我们开发了 RPA-CRISPR/Cas12a-G-四链体比色测定法,该方法可以与深度学习算法的智能识别相结合,实现 CaMV35S 启动子的灵敏、快速和便携检测。当 crRNA-Cas12a 复合物识别 RPA 扩增产物时,Cas12 会切割 G-四链体,导致 G4-血红素复合物失去过氧化物模拟酶功能,无法催化 ABTS 向 ABTS 的转化,从而可以根据 ABTS 吸光度来确定 CaMV35S 的浓度。通过利用 RPA-CRISPR/Cas12a-G4 测定法,我们实现了对 CaMV35S 的检测下限达到 10 aM,对 0.01%的基因修饰样本的检测时间为 45 分钟。深度学习算法被设计用于对颜色结果进行高度准确的分类。Yolov5 目标发现和 Resnet 分类算法已被训练用于比肉眼比色法更准确地识别痕量(0.01%)CaMV35S。我们还将深度学习算法与智能手机应用程序相结合,实现了便携和快速的照片识别。总的来说,我们的研究结果实现了低成本($0.43)、高准确性和智能化的 CaMV35S 启动子检测。

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