Label free colorimetric and fluorimetric direct detection of methylated DNA based on silver nanoclusters for cancer early diagnosis

被引:101
作者
Dadmehr, Mehdi [1 ]
Hosseini, Morteza [1 ]
Hosseinkhani, Saman [2 ]
Ganjali, Mohammad Reza [3 ,4 ]
Sheikhnejad, Reza [5 ]
机构
[1] Univ Tehran, Fac New Sci & Technol, Dept Life Sci Engn, Tehran, Iran
[2] Tarbiat Modares Univ, Dept Biochem, Tehran, Iran
[3] Univ Tehran, Fac Chem, Ctr Excellence Electrochem, Tehran, Iran
[4] Univ Tehran Med Sci, Endocrinol & Metab Mol Cellular Sci Inst, Biosensor Res Ctr, Tehran, Iran
[5] Tofigh Daru Co, Dept Mol Biol, Tehran, Iran
基金
美国国家科学基金会;
关键词
DNA methylation; Silver nanoclusters; Detection; Fluorescence; Cancer diagnosis; AG NANOCLUSTERS; 5-METHYLCYTOSINE; AMPLIFICATION; FLUOROPHORES; PATTERNS; CLEAVAGE; CLUSTERS; SEQ;
D O I
10.1016/j.bios.2015.05.062
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Epigenetic changes such as DNA methylation of CpG islands located in the promoter region of some tumor suppressor genes are very common in human diseases such as cancer. Detection of aberrant methylation pattern could serve as an excellent diagnostic approach. Recently, the direct detection of methylated DNA sequences without using chemical and enzymatic treatments or antibodies has received great deal of attentions. In this study, we report a calorimetric and fluorimetric technique for direct detection of DNA methylation. Here, the DNA is being used as an effective template for fluorescent silver nanoclusters formation without any chemical modification or DNA labeling. The sensitivity test showed that upon the addition of target methylated DNA, the fluorescence intensity is decreased in a linear range when the concentration of methylated DNA has increased from 2.0 x 10(-9) to 6.3 x 10(-7) M with the detection limit of 9.4 x 10(-10) M. The optical and fluorescence spectral behaviors were highly reproducible and clearly discriminated between unmethylated, methylated and even partially methylated DNA in CpG rich sequences. The results were also reproducible when the human plasma was present in our assay system. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:108 / 113
页数:6
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