College of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou 310027, China.
Sir Run-Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou 310016, China.
Biosensors (Basel). 2022 Mar 4;12(3):162. doi: 10.3390/bios12030162.
Aberrations of genomic DNA methylation have been confirmed to be involved in the evolution of human cancer and have thus gained the potential to be depicted as biomarkers for cancer diagnostics and prognostic predictions, which implicates an urgent need for detection of total genomic DNA methylation. In this work, we suggested an assay for the quantification of global DNA methylation, utilizing methylation specific antibody (5mC) modified magnetic beads (MBs) for immunorecognition and affinity enrichment. Subsequently, the captured DNA on the surface of MBs interacted with the glucose oxidase-conjugated DNA antibody whose catalytic reaction product was engaged in electrochemical detection of the overall level of DNA methylation on a PB-doped screen-printed electrode. With 15 pg of input DNA, which, to our best knowledge, is the lowest required amount of DNA without sodium bisulfite treatment or amplification, this test strategy was able to perceive as low as 5% methylation level within 70 min including the preparation of anti-5mC-MBs. We believe this detection technique offers a promising option to detect global DNA methylation in both academic and clinical scenarios.
基因组 DNA 甲基化的改变已被证实参与了人类癌症的演进,因此有可能被描绘为癌症诊断和预后预测的生物标志物,这意味着迫切需要检测总基因组 DNA 甲基化。在这项工作中,我们提出了一种用于定量检测全基因组 DNA 甲基化的方法,利用 5-甲基胞嘧啶(5mC)修饰的磁珠(MBs)进行免疫识别和亲和富集。随后,MBs 表面上捕获的 DNA 与葡萄糖氧化酶偶联的 DNA 抗体相互作用,其催化反应产物用于电化学检测 PB 掺杂的丝网印刷电极上总 DNA 甲基化水平。在我们的认知范围内,该测试策略仅需 15pg 的输入 DNA(无需亚硫酸氢钠处理或扩增),即可在 70 分钟内检测到低至 5%的甲基化水平,包括抗 5mC-MBs 的制备。我们相信,这种检测技术在学术和临床环境中都提供了一种有前途的检测全基因组 DNA 甲基化的方法。