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设计并优化用于基于适配体的侧向流动分析的金纳米颗粒 - cDNA纳米探针:应用于啶虫脒的快速检测。

Design and optimizing gold nanoparticle-cDNA nanoprobes for aptamer-based lateral flow assay: Application to rapid detection of acetamiprid.

作者信息

Mao Minxin, Xie Zhengjun, Ma Pengfei, Peng Chifang, Wang Zhouping, Wei Xinlin, Liu Guodong

机构信息

State Key Laboratory of Food Science and Technology, Jiangnan University, Lihu Road 1800, Wuxi, 214122, PR China.

School of Food Science and Technology, Jiangnan University, Lihu Road 1800, Wuxi, 214122, PR China.

出版信息

Biosens Bioelectron. 2022 Jul 1;207:114114. doi: 10.1016/j.bios.2022.114114. Epub 2022 Feb 26.

Abstract

The aptamer-based lateral flow assay strips (Apt-LFAs) have shown promising application prospects in the detection of small molecules. The general principle of Apt-LFAs used for the detection of small molecules is based on the target-induced dissociation (TID) competitive binding among the aptamer, target and gold nanoparticle (AuNP)-complementary DNA (cDNA) nanoprobes. One of the most important components in this device is AuNP-cDNA nanoprobe, which has strong effect on the sensitivity and specificity of Apt-LFAs. In this report, we designed an AuNPs@polyA-cDNA nanoprobe, which consists of a poly adenine (polyA) anchor blocker, a partial complementary DNA fragment to aptamer strand (cDNAa) and complementary DNA fragment to control DNA strand (cDNAc), for rapid detection of acetamiprid. cDNAa of AuNPs@polyA-cDNA nanoprobe was carefully investigated in terms of the hybridization site and length with the aptamer. A specific cDNAa sequence containing key binding bases of acetamiprid aptamer was obtained and verified by molecular docking analysis. After systematic optimization, the Apt-LFA was able to detect a minimum concentration of 0.33 ng mL acetamiprid. The Apt-LFA was successfully applied to detect spiked acetamiprid in tomato and rape samples with the recoveries ranged from 94 to 106%. Based on the strong versatility and verified molecular interaction mechanism, the design strategy could be extended to develop various Apt-LFAs for other small molecules.

摘要

基于适配体的侧向流动分析试纸条(Apt-LFAs)在小分子检测中显示出了广阔的应用前景。用于小分子检测的Apt-LFAs的一般原理基于适配体、靶标和金纳米颗粒(AuNP)-互补DNA(cDNA)纳米探针之间的靶标诱导解离(TID)竞争结合。该检测装置中最重要的组件之一是AuNP-cDNA纳米探针,它对Apt-LFAs的灵敏度和特异性有很大影响。在本报告中,我们设计了一种AuNPs@polyA-cDNA纳米探针,其由聚腺嘌呤(polyA)锚定阻断剂、与适配体链部分互补的DNA片段(cDNAa)和与对照DNA链互补的DNA片段(cDNAc)组成,用于快速检测啶虫脒。对AuNPs@polyA-cDNA纳米探针的cDNAa在与适配体的杂交位点和长度方面进行了仔细研究。通过分子对接分析获得并验证了包含啶虫脒适配体关键结合碱基的特定cDNAa序列。经过系统优化后,Apt-LFAs能够检测到最低浓度为0.33 ng/mL的啶虫脒。该Apt-LFAs成功应用于检测番茄和油菜样品中添加的啶虫脒,回收率在94%至106%之间。基于强大的通用性和经过验证的分子相互作用机制,该设计策略可扩展用于开发针对其他小分子的各种Apt-LFAs。

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