College of Electronic Information and Optical Engineering, Nankai University, Tianjin, China.
Analyst. 2019 Aug 5;144(16):4787-4794. doi: 10.1039/c9an00993k.
The applications of graphene field-effect transistors (FETs) for monitoring DNA hybridization have been widely accepted; however, for evaluating DNA methylation degree, an emerging requirement of epigenetic research, no work has been found due to the difficulties in detecting 5-methylcytosine (5mC) sites along the genomic sequence as well as counting their amount (NmC). Herein, to achieve this, a strategy for exploiting a liquid exfoliated graphene (LEG)-based FET (LEG-FET) as a sensing platform was proposed. First, LEG-FETs were prepared and activated by tetra-4-aminophenyl-porphyrin (TAPP) for anchoring single-strand DNAs (ssDNAs). Second, the 5mC sites in ssDNA were recognized by the specifically absorbed 5mC antibody (5mCab) and transduced to the changed currents (ΔIDS) by LEG-FET according to the integration of the methylation-immuno sensing principle and FET's working mechanism. Briefly, more 5mCab molecules could be captured by more 5mC sites, resulting in larger ΔIDS. The TAPP effects on LEG-FET were analyzed by SEM, Raman, AFM, and XPS characterizations as well as electronic measurements. The validity of this LEG-FET sensing platform for evaluating DNA methylation degree was proven step by step; this included the examinations of the synthesized ssDNAs with the known NmC and real ssDNA samples, whose methylation degrees were pre-determined by the gold-standard method, which is based on tedious bisulphite sequence operations and expensive mass spectrometry technology. Moreover, theoretical explanations were also provided for the sensing mechanism in the proposed DNA methylation analytical components. In conclusion, the positive and linear relations of IDS changing ratio vs. NmC as well as the detection limit of one 5mC site indicate that TAPP-modified LEG-FET can provide an alternative analytical tool to realize fast and economical DNA methylation evaluation.
石墨烯场效应晶体管(FET)在监测 DNA 杂交方面的应用已被广泛接受;然而,对于评估 DNA 甲基化程度,这是表观遗传学研究的新兴需求,由于难以检测基因组序列中 5-甲基胞嘧啶(5mC)位点以及计数其数量(NmC),因此尚未发现相关工作。在此,为了实现这一目标,提出了一种利用液相剥离石墨烯(LEG)基 FET(LEG-FET)作为传感平台的策略。首先,通过四-4-氨基苯基-卟啉(TAPP)对 LEG-FET 进行预处理和激活,以固定单链 DNA(ssDNA)。其次,ssDNA 中的 5mC 位点通过特异性结合的 5mC 抗体(5mCab)被识别,并根据甲基化免疫传感原理和 FET 的工作机制,将其转化为 LEG-FET 的电流变化(ΔIDS)。简而言之,更多的 5mCab 分子可以被更多的 5mC 位点捕获,从而导致更大的 ΔIDS。通过 SEM、Raman、AFM 和 XPS 表征以及电子测量分析了 TAPP 对 LEG-FET 的影响。通过逐步验证该 LEG-FET 传感平台评估 DNA 甲基化程度的有效性,包括对具有已知 NmC 的合成 ssDNA 以及通过繁琐的亚硫酸氢盐测序操作和昂贵的质谱技术预先确定了甲基化程度的真实 ssDNA 样本的检测。此外,还为所提出的 DNA 甲基化分析组件中的传感机制提供了理论解释。总之,IDS 变化率与 NmC 的正线性关系以及一个 5mC 位点的检测限表明,TAPP 修饰的 LEG-FET 可以提供一种替代的分析工具,以实现快速和经济的 DNA 甲基化评估。