Femtomolar level detection of RASSF1A tumor suppressor gene methylation by electrochemical nano-genosensor based on Fe 3 O 4 /TMC/Au nanocomposite and PT-modified electrode

微分脉冲伏安法 检出限 DNA甲基化 甲基化 DNA 化学 循环伏安法 纳米复合材料 分子生物学 电极 电化学 DNA微阵列 分析化学(期刊) 基因 材料科学 色谱法 纳米技术 生物 生物化学 基因表达 物理化学
作者
Maryam S. Daneshpour,Leila Moradi,Pantea Izadi,Kobra Omidfar
出处
期刊:Biosensors and Bioelectronics [Elsevier]
卷期号:77: 1095-1103 被引量:65
标识
DOI:10.1016/j.bios.2015.11.007
摘要

The alterations in DNA methylation pattern have been identified as one of the most frequent molecular phenomenon in human cancers. The RASSF1A tumor suppressor gene was shown to be often inactivated by hypermethylation of its promoter region. In the present study, a novel chip format sandwich electrochemical genosensor has been developed for the analysis of gene-specific methylation using Fe3O4/N-trimethyl chitosan/gold (Fe3O4/TMC/Au) nanocomposite as tracing tag to label DNA probe and polythiophene (PT) as immobilization platform of sensing element. However, no attempt has yet been made to conjugate DNA probe to Fe3O4/TMC/Au nanocomposite as electrochemical label for strip-based genosensing. Cyclic voltammetric (CV) analysis indicated that modification procedure was well performed. Differential pulse voltammetry (DPV) was employed for quantitative assessment of RASSF1A DNA promoter methylation. The electrochemical measurements accomplished using non-specific DNA fragments mixed with samples, revealed the high specificity and selectivity in methylation analysis by means of this DNA nanobiosensor. With the linear range of concentration from 1 × 10(-14)M to 5 × 10(-9)M and the detection limit of 2 × 10(-15)M, this new strategy has shown such a promising application to be used for universal analysis of any DNA sequence.

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