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Exonuclease III-assisted strand displacement reaction-driven cyclic generation of G-quadruplex strategy for homogeneous fluorescent detection of melamine.

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机构: [a]Department of Laboratory Medicine, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center for Biotherapy. Chengdu, Sichuan, 610041, China [b]College of Chemistry and Material Science, Sichuan Normal University, Chengdu, Sichuan, 610068, China [c]School of Pharmaceutical Sciences, Guangzhou Higher Education Mega Center, Sun Yat-sen University, Guangzhou, 510006, China [d]Shenzhen Institute of Geriatrics, Shenzhen, The First Affiliated Hospital of Shenzhen University, Health Science Center,The Second People's Hospital of Shenzhen,Shenzhen, 518035, China
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关键词: Melamine Thymine-melamine-thymine G-quadruplex-NMM Strand displacement amplification Exonuclease III Fluorescence

摘要:
Development of flexible, sensitive, selective and simple melamine detection is in high demand and of great significance. Here, we proposed a homogeneous turn-off mode fluorescent strategy to detect melamine by coupling the process of exonuclease III-assisted (Exo III) amplification with the strand displacement reaction (SDR)-driven assembly of DNA G-quadruplex structures. Melamine (M) could bind to the thymine (T) base through hydrogen bonding to form a T-M-T structure, which inhibits the subsequent nucleic acid amplification reaction and formation of the G-quadruplex structure. DNA strand (G1) served as both a recognition probe and a signal probe, thus greatly simplifying the experimental design and operation. Furthermore, to improve the detection sensitivity, an ingeniously designed segment of double-stranded DNA (dsDNA, P1-G2) that contained the G-quadruplex sequence (G2) and a partially hybridized signal trigger strand (P1) was added to the system. Following the SDR and Exo III-assisted amplification, G1-DNA and G2-DNA were released and the cyclic production of G-quadruplex structures was initiated. The generated DNA G-quadruplex bound to the NMM (a fluorescent dye, N-methyl mesoporphyrin IX), providing enhanced fluorescence signals. This allowed for the highly sensitive detection of melamine at concentrations as low as 25 fM. The proposed fluorescent detection method of melamine concentration displayed a good linear relationship ranging from 100 fM to 100 pM, which showed improved performance over that of the non-enzyme-assisted sensing system (limit of detection is 15 pM). Additionally, this method exhibited a high selectivity towards the target molecule, melamine, in comparison to other substances. Furthermore, the method was used for the assay of melamine in real milk samples and satisfactory experiment results were obtained. The novel strategy developed in this research may be considered as a potential route for highly sensitive, simple, selective and accurate assay of small molecules. Copyright © 2019 Elsevier B.V. All rights reserved.

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出版当年[2019]版:
大类 | 2 区 化学
小类 | 1 区 分析化学
最新[2023]版:
大类 | 1 区 化学
小类 | 1 区 分析化学
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出版当年[2019]版:
Q1 CHEMISTRY, ANALYTICAL
最新[2023]版:
Q1 CHEMISTRY, ANALYTICAL

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第一作者机构: [a]Department of Laboratory Medicine, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center for Biotherapy. Chengdu, Sichuan, 610041, China
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