Abstract
Herein, we report that the ternary chalcogenide nanosheet exhibits different affinity toward oligonucleotides with different lengths and efficiently quenches the fluorescence of dye-labeled DNA probes. Based on these findings, as a proof-of-concept application, the ternary chalcogenide nanosheet is used as a target cyclic amplification biosensor, showing high specificity in discriminating single-base mismatch. This simple strategy is fast and sensitive for the single nucleotide polymorphism detection. Ultralow detection limit of unlabeled target (250 fM) and high discrimination ratio (5%) in the mixture of perfect match (mutant-type) and single-base mismatch (wild-type) target are achieved. This sensing method is extensively compatible for the single nucleotide polymorphism detection in clinical samples, making it a promising tool for the mutation-based clinical diagnostic and genomic research. © Copyright © 2019 Hu, Tan, Lin, Lai, Zhang, Lu, Feng, Yang and Weng.
| Original language | English |
|---|---|
| Article number | 844 |
| Journal | Frontiers in Chemistry |
| Volume | 7 |
| DOIs | |
| Publication status | Published - 6 Dec 2019 |
| Externally published | Yes |
Research Keywords
- fluorescent detection
- sensor
- single nucleotide polymorphisms
- ternary chalcogenide nanosheets
- two-dimensional nanomaterials
Publisher's Copyright Statement
- This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/
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