Exonuclease III-regulated target cyclic amplification-based single nucleotide polymorphism detection using ultrathin ternary chalcogenide nanosheets

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...

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Main Authors: Hu, Yanling, Tan, Chaoliang, Lin, Xin, Lai, Zhuangchai, Zhang, Xiao, Lu, Qipeng, Feng, Ning, Yang, Dongliang, Weng, Lixing
Other Authors: School of Materials Science and Engineering
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/145542
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1455422023-07-14T15:53:06Z Exonuclease III-regulated target cyclic amplification-based single nucleotide polymorphism detection using ultrathin ternary chalcogenide nanosheets Hu, Yanling Tan, Chaoliang Lin, Xin Lai, Zhuangchai Zhang, Xiao Lu, Qipeng Feng, Ning Yang, Dongliang Weng, Lixing School of Materials Science and Engineering Science::Chemistry Ternary Chalcogenide Nanosheets Single Nucleotide Polymorphisms 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. Published version 2020-12-28T04:15:19Z 2020-12-28T04:15:19Z 2019 Journal Article Hu, Y., Tan, C., Lin, X., Lai, Z., Zhang, X., Lu, Q., . . . Weng, L. (2019). Exonuclease III-regulated target cyclic amplification-based single nucleotide polymorphism detection using ultrathin ternary chalcogenide nanosheets. Frontiers in Chemistry, 7, 844-. doi:10.3389/fchem.2019.00844 2296-2646 https://hdl.handle.net/10356/145542 10.3389/fchem.2019.00844 31921768 7 en Frontiers in Chemistry © 2019 Hu, Tan, Lin, Lai, Zhang, Lu, Feng, Yang and Weng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry
Ternary Chalcogenide Nanosheets
Single Nucleotide Polymorphisms
spellingShingle Science::Chemistry
Ternary Chalcogenide Nanosheets
Single Nucleotide Polymorphisms
Hu, Yanling
Tan, Chaoliang
Lin, Xin
Lai, Zhuangchai
Zhang, Xiao
Lu, Qipeng
Feng, Ning
Yang, Dongliang
Weng, Lixing
Exonuclease III-regulated target cyclic amplification-based single nucleotide polymorphism detection using ultrathin ternary chalcogenide nanosheets
description 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.
author2 School of Materials Science and Engineering
author_facet School of Materials Science and Engineering
Hu, Yanling
Tan, Chaoliang
Lin, Xin
Lai, Zhuangchai
Zhang, Xiao
Lu, Qipeng
Feng, Ning
Yang, Dongliang
Weng, Lixing
format Article
author Hu, Yanling
Tan, Chaoliang
Lin, Xin
Lai, Zhuangchai
Zhang, Xiao
Lu, Qipeng
Feng, Ning
Yang, Dongliang
Weng, Lixing
author_sort Hu, Yanling
title Exonuclease III-regulated target cyclic amplification-based single nucleotide polymorphism detection using ultrathin ternary chalcogenide nanosheets
title_short Exonuclease III-regulated target cyclic amplification-based single nucleotide polymorphism detection using ultrathin ternary chalcogenide nanosheets
title_full Exonuclease III-regulated target cyclic amplification-based single nucleotide polymorphism detection using ultrathin ternary chalcogenide nanosheets
title_fullStr Exonuclease III-regulated target cyclic amplification-based single nucleotide polymorphism detection using ultrathin ternary chalcogenide nanosheets
title_full_unstemmed Exonuclease III-regulated target cyclic amplification-based single nucleotide polymorphism detection using ultrathin ternary chalcogenide nanosheets
title_sort exonuclease iii-regulated target cyclic amplification-based single nucleotide polymorphism detection using ultrathin ternary chalcogenide nanosheets
publishDate 2020
url https://hdl.handle.net/10356/145542
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