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Electrochemical DNA Methylation Detection for Enzymatically Digested CpG Oligonucleotides

机译:酶消化的CpG寡核苷酸的电化学DNA甲基化检测

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We describe the electrochemical detection of DNA methylation through the direct oxidation of both 5-methylcytosine (mC) and cytosine (C) in 5'-CG-3' sequence (CpG) oligonucleotides using a sputtered nanocarbon film electrode after digesting a longer CpG oligonucleotide with endonuclease P1. Direct electrochemistry of the longer CpG oligonucleotides was insufficient for obtaining the oxidation currents of these bases because the CG rich sequence inhibited the direct oxidation of each base in the longer CpG oligonucleotides, owing to the conformational structure and its very low diffusion coefficient. To detect C methylation with better quantitativity and sensitivity in the relatively long CpG oligonucleotides, we successfully used an endonuclease P1 to digest the target CpG oligonucleotide and yield an identical mononucleotide 2'-deoxyribonucleoside 5'-monophosphate (5'-dNMP). Compared with results obtained without P1 treatment, we achieved 4.4 times higher sensitivity and a wider concentration range for mC detection with a resolution capable of detecting a subtle methylated cytosine difference in the CpG oligonucleotides (60mer).
机译:我们描述了通过消化更长的CpG寡核苷酸后使用溅射的纳米碳膜电极通过5'-CG-3'序列(CpG)寡核苷酸中的5-甲基胞嘧啶(mC)和胞嘧啶(C)的直接氧化来电化学检测DNA甲基化用核酸内切酶P1。较长的CpG寡核苷酸的直接电化学不足以获得这些碱基的氧化电流,因为富含CG的序列由于构象结构及其极低的扩散系数而抑制了较长的CpG寡核苷酸中每个碱基的直接氧化。为了在相对较长的CpG寡核苷酸中以更好的定量和灵敏度检测C甲基化,我们成功地使用核酸内切酶P1消化了目标CpG寡核苷酸,并产生了相同的单核苷酸2'-脱氧核糖核苷5'-单磷酸酯(5'-dNMP)。与未经P1处理的结果相比,我们实现了4.4倍的mC检测灵敏度和更宽的浓度范围,并且具有能够检测CpG寡核苷酸(60mer)中微妙的甲基化胞嘧啶差异的分辨率。

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