Abstract
A method is presented that uses photoinduced electron transfer (PET) for the determination of microRNAs (miRNAs) in clinical serum samples and complicated cell samples by using a smartphone. miRNA-21 is adopted as a model analyte. A 3′-phosphorylated DNA probe containing AgNCs is synthesized and hybridized with miRNA-21. Subsequently, the probe is cleaved specifically by duplex-specific nuclease to form 3′-hydroxylated products, then extended by terminal deoxynucleotidyl transferase (TdT) with superlong G for G-quadruplex/hemin units fabrication. In this way, PET occurred between AgNCs and produced G-quadruplex/hemin units, leading to the fluorescence quenching of AgNCs. Notably, the fluorescence images can be captured and translated into digital information by smartphone, resulting in a direct quantitative determination of miRNA. As a result, our strategy for miRNA assay is achieved with a satisfactory detection limit of 1.43 pM. Interestingly, TdT-propelled G-quadruplex/hemin units as multiple electron acceptors promote the sensitivity of miRNA monitoring. Different miRNAs assays are realized by adjusting the complimentary sequences of DNA probe. These qualities not only broaden the practical application of PET-based strategy, but also provide a new insight into the nucleic acid detection.
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Funding
This work is financially supported by the National Natural Science Foundation of China (Grant Nos. 31800670 and 21603003), the Key Project of Natural Science Foundation of Anhui Provincial Department of Education (Grant No. KJ2019A0583), and the Foundation of State Key Laboratory of High-efficiency Utilization of Coal and Green Chemical Engineering (Grant No. 2018-K34).
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Yang, Y., Liu, S., Cui, X. et al. Sensitive detection of miRNA based on enzyme-propelled multiple photoinduced electron transfer strategy. Microchim Acta 188, 219 (2021). https://doi.org/10.1007/s00604-021-04874-2
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DOI: https://doi.org/10.1007/s00604-021-04874-2