期刊
ACS SENSORS
卷 8, 期 4, 页码 1579-1584出版社
AMER CHEMICAL SOC
DOI: 10.1021/acssensors.2c02695
关键词
electrochemiluminescence; biosensor; toxin determination; aggregation-induced enhancement; nanocluster; DNA amplification strategy
In this study, an electrochemiluminescence (ECL) biosensor was developed for ultra-sensitive detection of the halogenase gene segment from aspergillus ochratoxin, using aggregation-induced enhancement ECL of Ag nanoribbons (Ag NRs) as a signal probe and mismatched bases-fueled DNA walker as the amplification strategy. The Ag NRs exhibited greatly enhanced ECL emission due to effective electron transfer and less energy dissipation, thanks to the metallophilic interaction of Ag(I)-Ag(I). The strategy realized trace analysis of the target gene segment with a detection limit of 45 aM, providing a new method for toxin determination in the early stage of toxin biosynthesis to protect people from toxic damage.
Here, an electrochemiluminescence (ECL) biosensor was developed based on aggregation-induced enhancement ECL of Ag nanoribbons (Ag NRs) as a signal probe and the mismatched bases-fueled DNA walker as the amplification strategy for ultra sensitive detection of the halogenase gene segment (target) from aspergillus ochratoxin to evaluate fungi capable of producing ochratoxin in dairy products. Compared with the existing agminated NCs, the Ag NRs displayed dramatically enhanced ECL emission due to effective electron transfer and less energy dissipation of excited-state Ag NRs based on the metallophilic interaction of Ag(I)-Ag(I). Impressively, the target was conversed mismatched bases-DNA walker to trigger a significant ECL response through toehold-mediated strand displacement amplification. Thus, the strategy realized trace analysis of the halogenase gene segment with a detection limit of 45 aM, which ushered a new detection method for toxin determination in the previous stage of toxin biosynthesis to protect people from toxic damage.
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