Rapid restriction enzyme free detection of DNA methyltransferase activity based on DNA-templated silver nanoclusters

被引:53
作者
Kermani, Hanie Ahmadzade [1 ]
Hosseini, Morteza [1 ]
Dadmehr, Mehdi [2 ]
Ganjali, Mohammad Reza [3 ]
机构
[1] Univ Tehran, Dept Life Sci Engn, Fac New Sci & Technol, Tehran 1417466191, Iran
[2] Payame Noor Univ, Dept Biotechnol, Tehran 193954697, Iran
[3] Univ Tehran, Fac Chem, Ctr Excellence Electrochem, Tehran 1417466191, Iran
关键词
DNA methyltransferase enzyme; Silver nanoclusters; Fluorescence assay; M.SssI activity; SIGNAL AMPLIFICATION; METHYLATION DETECTION; FLUORESCENT ASSAY; ENDONUCLEASE; PROBE; INHIBITION; PROTEIN; CANCER; DNAZYME; DISEASE;
D O I
10.1007/s00216-016-9522-z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
DNA methylation has significant roles in gene regulation. DNA methyltransferase (MTase) enzyme characterizes DNA methylation and also induces an aberrant methylation pattern that is related to many diseases, especially cancers. Thus, it is required to develop a method to detect the DNA MTase activity. In this study, we developed a new sensitive and reliable method for methyltransferase activity assay by employing DNA-templated silver nanoclusters (DNA/Ag NCs) without using restriction enzymes. The Ag NCs have been utilized for the determination of M.SssI MTase activity and its inhibition. We designed an oligonucleotide probe which contained an inserted six-cytosine loop as Ag NCs formation template. The changes in fluorescence intensity were monitored to quantify the M.SssI activity. The fluorescence spectra showed a linear decrease in the range of 0.4 to 20 U/ml with a detection limit of 0.1 U/ml, which was significant compared with previous reports. The proposed method was applied successfully for demonstrating the Gentamicin effect as MTase inhibitor. The proposed method showed convenient reproducibility and sensitivity indicating its potential for the determination of methyltransferase activity.
引用
收藏
页码:4311 / 4318
页数:8
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