Ultrasensitive strategy for OTA analysis by both recognition-activated multiple isothermal cyclic strand displacement amplification and DNAzyme-mediated cyclic signal reporting mechanism

脱氧核酶 适体 检出限 化学 环介导等温扩增 底漆(化妆品) 荧光 焦磷酸盐 信号(编程语言) 组合化学 生物物理学 DNA 计算机科学 色谱法 生物化学 分子生物学 物理 生物 量子力学 有机化学 程序设计语言
作者
Shiyi Wang,Qi Chen,Hang Wang,Qian Wu,Noor Fatima,Chao Yan,Bangben Yao,Wei Chen
出处
期刊:Sensors and Actuators B-chemical [Elsevier BV]
卷期号:420: 136418-136418 被引量:4
标识
DOI:10.1016/j.snb.2024.136418
摘要

We propose a recognition-driven ultrasensitive fluorescence sensing strategy for accurate analysis of ochratoxin A (OTA) by taking Mg 2+ -dependent DNAzyme based catalysis as the final signal output module. Recognition of target OTA destroys the simple double-strand recognition structure and contributes to the liberation of primer probe, which can trigger and activate the primer-mediated multiple isothermal cyclic strand displacement amplification (M-CSDA) process. The designed dual templates (T-P, T-A) can contribute to the generation of enormous nicked products (DNAzyme and primer), which will take effect in the triggering of M-CSDA. Meanwhile, one of the nicked products (DNAzyme) will also take part in the cyclically cleavage of designed hairpin probes (HP) with the presence of the cofactor Mg 2+ , inducing the recovery of fluorescent signal of quenched hairpin probes. Only the trace amount of target OTA could generate drastic fluorescent signal and ultrasensitive detection of OTA could be well achieved. Under optimized conditions, the detection limit of this method for OTA is 0.59 fg/mL. The characteristics of this method including the simplicity in dual signal amplification design, isothermal operation process and easy fluorescence measurement model exhibit the superior sensitivity and specificity for OTA detection. And this strategy can be further expanded for the design of ultrasensitive aptamer-sensing methods for series analytes. • Aptamer-mediated M-CSDA sensing strategy constructed for ultrasensitive detection of OTA. • OTA recognition activated the multiple isothermal cyclic strand displacement amplification signal amplification module. • M-CSDA initiated the DNAzyme-mediated cyclic signal reporting module for signal output. • As low as 0.59 fg/mL achieved for OTA detection in the simple-operational way. • Practical applications of aptamer-mediated M-CSDA sensing strategy in real samples well performed.
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