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Direct DNA Methylation Profiling with an Electric Biosensor

机译:用电生体传感器直接DNA甲基化分析

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摘要

DNA methylation is one of the principal epigenetic mechanisms that control gene expression in humans, and its profiling provides critical information about health and disease. Current profiling methods require chemical modification of bases followed by sequencing, which is expensive and time-consuming. Here, we report a direct and rapid determination of DNA methylation using an electric biosensor. The device consists of a DNA-tweezer probe integrated on a graphene field-effect transistor for label-free, highly sensitive, and specific methylation profiling. The device performance was evaluated with a target DNA that harbors a sequence of the methylguanine-DNA methyltransferase, a promoter of glioblastoma multiforme, a lethal brain tumor. The results show that we successfully profiled the methylated and nonmethylated forms at picomolar concentrations. Further, fluorescence kinetics and molecular dynamics simulations revealed that the position of the methylation site(s), their proximity, and accessibility to the toe-hold region of the tweezer probe are the primary determinants of the device performance.
机译:DNA甲基化是对人类中基因表达的主要表观遗传机制之一,其分析提供了有关健康和疾病的关键信息。电流分析方法需要碱的化学改性,然后进行测序,这昂贵且耗时。在这里,我们通过电生物传感器报告DNA甲基化的直接和快速测定。该装置包括集成在石墨烯场效应晶体管上的DNA-Tweezer探针,用于无标记,高敏感和特定的甲基化分析。用靶向DNA评价器件性能,该靶DNA将甲基胍-DNA甲基转移酶的序列,胶质母细胞瘤多形形的促进剂,致死的脑肿瘤。结果表明,我们成功地以皮摩尔浓度成功地分析了甲基化和非甲基化形式。此外,荧光动力学和分子动力学模拟显示甲基化位点,其接近和对镊子探针的趾部区域的可触及的位置是器件性能的主要决定因素。

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