An integrated and restructive probe mediated strand displacement amplification strategy for sensitive and specific DNA methyltransferase activity detection

被引:17
|
作者
Xu, Xiaowen [1 ]
Wang, Lei [2 ]
Cui, Wanling [1 ]
Jiang, Wei [1 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Educ Minist, Key Lab Colloid & Interface Chem, Jinan 250100, Shandong, Peoples R China
[2] Shandong Univ, Sch Pharmaceut Sci, Jinan 250012, Shandong, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Integrated and restructive probe; Strand displacement amplification; DNA methyltransferase activity; Fluorescent detection; ROLLING CIRCLE AMPLIFICATION; ASSISTED SIGNAL AMPLIFICATION; HYBRIDIZATION CHAIN-REACTION; FLUORESCENCE ASSAY; DAM METHYLTRANSFERASE; ESCHERICHIA-COLI; METHYLATION; CLEAVAGE; CHEMILUMINESCENCE; DNAZYME;
D O I
10.1016/j.snb.2018.03.127
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein, an integrated and restructive probe mediated strand displacement amplification (SDA) strategy is developed for sensitive and specific DNA MTase activity detection. The probe is specially designed with a hairpin structure, which encloses the MTase recognition site in the stem and seals the SDA primer and template in the loop. Under the action of DNA MTase, the probe is methylated and cleaved by DpnI endonuclease, causing its stem truncated. The truncated structure then reconstructs with a shrunken loop and a partially-hybridized duplex of stem, drawing the SDA primer and template domains close to trigger cascade amplification. Numerous G-quadruplexes are produced and intercalated by N-methyl-mesoporphyrin IX (NMM) to generate enhanced fluorescent signal. This strategy detects MTase activity down to 0.063 U/mL, and well distinguishes Dam MTase from its analogues. It is further applied for the MTase detection in biological samples and MTase inhibition analysis. The strategy will provide a promising tool for detection MTase activity in biomedical study and early cancer diagnosis. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:124 / 130
页数:7
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