Department of Micro- and Nanotechnology DTU Nanotech, Technical University of Denmark , Building 345B, Kongens Lyngby, DK 2800, Denmark.
Division of Mechanical and Biomedical Engineering, ELTEC College of Engineering, Ewha Womans University , Seoul 03760, South Korea.
ACS Nano. 2017 Sep 26;11(9):8864-8870. doi: 10.1021/acsnano.7b03053. Epub 2017 Sep 13.
Epigenetic modifications, in particular DNA methylation, are gaining increasing interest as complementary information to DNA mutations for cancer diagnostics and prognostics. We introduce a method to simultaneously profile DNA mutation and methylation events for an array of sites with single site specificity. Genomic (mutation) or bisulphite-treated (methylation) DNA is amplified using nondiscriminatory primers, and the amplicons are then hybridized to a giant magnetoresistive (GMR) biosensor array followed by melting curve measurements. The GMR biosensor platform offers scalable multiplexed detection of DNA hybridization, which is insensitive to temperature variation. The melting curve approach further enhances the assay specificity and tolerance to variations in probe length. We demonstrate the utility of this method by simultaneously profiling five mutation and four methylation sites in human melanoma cell lines. The method correctly identified all mutation and methylation events and further provided quantitative assessment of methylation density validated by bisulphite pyrosequencing.
表观遗传修饰,特别是 DNA 甲基化,作为 DNA 突变的补充信息,在癌症诊断和预后方面越来越受到关注。我们介绍了一种方法,可以同时对具有单个位点特异性的一系列位点的 DNA 突变和甲基化事件进行分析。使用非歧视性引物扩增基因组(突变)或亚硫酸氢盐处理(甲基化)的 DNA,然后将扩增子杂交到巨磁电阻(GMR)生物传感器阵列上,然后进行熔解曲线测量。GMR 生物传感器平台提供了可扩展的 DNA 杂交多重检测,对温度变化不敏感。熔解曲线方法进一步提高了检测的特异性和对探针长度变化的容忍度。我们通过同时分析人类黑色素瘤细胞系中的五个突变和四个甲基化位点来证明该方法的实用性。该方法正确识别了所有的突变和甲基化事件,并进一步通过亚硫酸氢盐焦磷酸测序进行了定量评估,验证了甲基化密度。