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

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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Publication Details

Journal
Sensors and Actuators B Chemical
Published
2024-08-12
DOI
https://doi.org/10.1016/j.snb.2024.136418
Citations
4
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
0.94

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article

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

Shiyi Wang, Chao Yan, Wei Chen, Hang Wang et al.
4 citations
Sensors and Actuators B Chemical
Advanced biosensing and bioanalysis techniques
0.94
article

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

Shiyi Wang, Chao Yan, Wei Chen, Hang Wang, Noor Fatima, Qian Wu, Qi Chen, Bangben Yao
article en
4 citations

Abstract

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.

Sensors and Actuators B ChemicalVol. 420
Anhui University (CN), Hefei University of Technology (CN), China Agricultural University (CN)
Shanghai Municipal Health Commission, Department of Science and Technology, Ministry of Science and Technology, India, National Natural Science Foundation of China, Key Research and Development Project of Hainan Province, Key Program of NSFC-Tongyong Union Foundation, Anhui Provincial Key Research and Development Plan, Budget Division
Openalex Percentile: Top 26%
Advanced biosensing and bioanalysis techniques
0.94
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