Zhu Quanjing, Yang Haoyang, Luo Jing, Huang Hui, Fang Lichao, Deng Jun, Li Chenghong, Li Yan, Zeng Tao, Zheng Junsong
Department of Clinical and Military Laboratory Medicine, College of Medical Laboratory Science, Army Medical University, 30 Gaotanyan Street, Shapingba District, Chongqing, 400038, PR China.
Department of Clinical and Military Laboratory Medicine, College of Medical Laboratory Science, Army Medical University, 30 Gaotanyan Street, Shapingba District, Chongqing, 400038, PR China.
Anal Chim Acta. 2021 Jan 15;1142:127-134. doi: 10.1016/j.aca.2020.10.064. Epub 2020 Nov 5.
DNA methylation plays an important role in a variety of human diseases. Thus, accurately analyze 5-methylcytosine in different DNA segments is of great significance. Herein, we proposed a novel 3D matrixed DNA self-nanocatalyzer via gold nanoparticles (AuNPs) supporting DNA self-hybridization with hemin as biomimetic enzyme and methylene blue (MB) as electrochemical mediator, which was employed as an efficient electrochemical sensitizer for the ultrasensitive bioassay of DNA 5-methylcytosine. Meanwhile, the AuNPs, graphitic carbon nitride (g-CN) and reduced graphene oxide (rGO) was prepared as AuNPs/g-CN@rGO nanocomposites to coat on the electrode surface to immobilize the capture hairpin DNA (CH). In the presence of target DNA with 5-methylcytosine, the target DNA could hybridize with CH via the hyperstable triple-helix formation. Based on the specific biorecognition between biotin and streptavidin and immune recognition between anti-5-methylcytosine antibodies and 5-methylcytosine sites on the target DNA, the 3D matrixed DNA self-nanocatalyzer could be captured onto the electrode surface to generate an amplified electrochemical signal related to the concentration of 5-methylcytosine. Under the optimal conditions, the proposed strategy performed a linear range from 10 M to 10 M with a detection limit of 8.6 aM. Remarkably, this strategy could be expanded easily to various biomarkers, including protein, DNA, phosphorylation and glycosylation, providing a promising strategy for clinical diagnosis and mechanism investigation of various diseases.
DNA甲基化在多种人类疾病中发挥着重要作用。因此,准确分析不同DNA片段中的5-甲基胞嘧啶具有重要意义。在此,我们通过金纳米颗粒(AuNPs)支持DNA自杂交,以血红素作为仿生酶,亚甲基蓝(MB)作为电化学介质,提出了一种新型的三维矩阵DNA自纳米催化剂,其被用作DNA 5-甲基胞嘧啶超灵敏生物检测的高效电化学增敏剂。同时,制备了AuNPs、石墨相氮化碳(g-CN)和还原氧化石墨烯(rGO)作为AuNPs/g-CN@rGO纳米复合材料,涂覆在电极表面以固定捕获发夹DNA(CH)。在存在含5-甲基胞嘧啶的靶DNA时,靶DNA可通过形成超稳定的三螺旋与CH杂交。基于生物素与链霉亲和素之间的特异性生物识别以及抗5-甲基胞嘧啶抗体与靶DNA上5-甲基胞嘧啶位点之间的免疫识别,三维矩阵DNA自纳米催化剂可被捕获到电极表面,以产生与5-甲基胞嘧啶浓度相关的放大电化学信号。在最佳条件下,所提出的策略的线性范围为10⁻¹² M至10⁻⁸ M,检测限为8.6 aM。值得注意的是,该策略可轻松扩展到各种生物标志物,包括蛋白质、DNA、磷酸化和糖基化,为各种疾病的临床诊断和机制研究提供了一种有前景的策略。