TY - JOUR
T1 - Exonuclease III-Regulated Target Cyclic Amplification-Based Single Nucleotide Polymorphism Detection Using Ultrathin Ternary Chalcogenide Nanosheets
AU - Hu, Yanling
AU - Tan, Chaoliang
AU - Lin, Xin
AU - Lai, Zhuangchai
AU - Zhang, Xiao
AU - Lu, Qipeng
AU - Feng, Ning
AU - Yang, Dongliang
AU - Weng, Lixing
N1 - Publisher Copyright:
© Copyright © 2019 Hu, Tan, Lin, Lai, Zhang, Lu, Feng, Yang and Weng.
PY - 2019/12/6
Y1 - 2019/12/6
N2 - 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.
AB - 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.
KW - fluorescent detection
KW - sensor
KW - single nucleotide polymorphisms
KW - ternary chalcogenide nanosheets
KW - two-dimensional nanomaterials
UR - http://www.scopus.com/inward/record.url?scp=85077242805&partnerID=8YFLogxK
U2 - 10.3389/fchem.2019.00844
DO - 10.3389/fchem.2019.00844
M3 - 文章
AN - SCOPUS:85077242805
SN - 2296-2646
VL - 7
JO - Frontiers in Chemistry
JF - Frontiers in Chemistry
M1 - 844
ER -