An all-in-one enzyme-free fluorescent aptasensor integrating localized catalyzed hairpin assembly for sensing antibiotics in food with improved detection efficiency.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Yuanyuan Peng, Min Wu, Min Liu, Yushu Wu
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Abstract

Enzyme-free signal amplification fluorescent aptasensors depending on multi-component freely diffusing probes have become indispensable tools for antibiotic detection in food, but they suffer from low detection efficiency and tedious operation steps. Herein, an all-in-one enzyme-free fluorescent aptasensor integrating localized catalyzed hairpin assembly (L-CHA) was designed for antibiotic detection with improved detection efficiency. In the designed aptasensor, a double-stranded DNA reactant containing an antibiotic aptamer and a primer as well as two paired hairpin DNA reactants were immobilized on one spatial-confinement DNA scaffold (that is a DNA tetrahedron). Upon addition of the target antibiotic kanamycin, the activated primer initiated L-CHA, generating an amplified fluorescence signal. Compared with previously reported enzyme-free signal amplification fluorescent aptasensors, the designed aptasensor integrated the functions of target recognition, signal transduction, and L-CHA signal amplification into a single probe. In this all-in-one design, the reactants in this aptasensor were confined to a compact space for a higher local concentration, which improved detection efficiency. In particular, this aptasensor achieved sensitive detection of kanamycin within 60 min with a low detection limit of 0.019 ng mL-1. Additionally, the designed aptasensor depended on a single probe rather than multi-component probes, leading to simplified operation steps. Furthermore, this aptasensor was employed for detecting kanamycin in spiked milk samples with recoveries of 96.00% to 108.60%, indicating an acceptable accuracy. Therefore, this L-CHA-based all-in-one enzyme-free fluorescent aptasensor offers a prospective tool for antibiotic detection in the field of food safety.

一种整合了局部催化发夹组装的一体化无酶荧光传感器,可用于感知食品中的抗生素并提高检测效率。
基于多组分自由扩散探针的无酶信号放大荧光传感器已成为食品中抗生素检测不可或缺的工具,但其存在检测效率低、操作步骤繁琐等问题。本文设计了一种整合了局部催化发夹组装(L-CHA)的一体化无酶荧光传感器,用于抗生素检测,提高了检测效率。在所设计的传感器中,含有抗生素适配体和引物的双链 DNA 反应物以及两个成对的发夹 DNA 反应物被固定在一个空间整合 DNA 支架(即 DNA 四面体)上。加入目标抗生素卡那霉素后,激活的引物启动 L-CHA,产生放大的荧光信号。与之前报道的无酶信号放大荧光诱导传感器相比,所设计的诱导传感器将目标识别、信号转导和 L-CHA 信号放大功能整合到了一个探针中。在这种一体化设计中,该传感器中的反应物被限制在一个紧凑的空间内,从而获得了更高的局部浓度,提高了检测效率。特别是,这种适配传感器可在 60 分钟内实现对卡那霉素的灵敏检测,检测限低至 0.019 ng mL-1。此外,所设计的适配传感器只需使用一个探针,而无需使用多组分探针,从而简化了操作步骤。此外,该传感器还可用于检测加标牛奶样品中的卡那霉素,其回收率为 96.00% 至 108.60%,准确度可接受。因此,这种基于 L-CHA 的一体化无酶荧光传感器为食品安全领域的抗生素检测提供了一种前景广阔的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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