Department of Chemistry, Nanchang University, Nanchang 330031, PR China.
Department of Chemistry, Nanchang University, Nanchang 330031, PR China.
Spectrochim Acta A Mol Biomol Spectrosc. 2021 Nov 5;260:119924. doi: 10.1016/j.saa.2021.119924. Epub 2021 May 7.
The assay of detecting DNA methyltransferase activity has been identified as one of the central challenges in cancer diagnostics as DNA methylation is closely related to the diagnosis and treatment of tumors. In this study, a label-free fluorescence probe based on poly-thymine copper nanoclusters engineered by terminal deoxynucleotidyl transferase is proposed for methyltransferase activity assay. Taking advantage of the efficient polymerization extension reaction catalyzed by terminal deoxynucleotidyl transferase and the copper nanoclusters with large Stokes shift instead of labeling fluorescent dyes, the strategy exhibits a broader linear scope from 1 to 300 U mL with a detection limit of 0.176 U mL. The economical method is specificity for M.SssI and also provides a convenient and high-throughput platform for screening the DNA methylation inhibitors, which displays a great potential for the practical applications of the drug development and clinical cancer diagnosis in the future.
检测 DNA 甲基转移酶活性的测定已被确定为癌症诊断中的核心挑战之一,因为 DNA 甲基化与肿瘤的诊断和治疗密切相关。在这项研究中,提出了一种基于末端脱氧核苷酸转移酶工程化的聚胸腺嘧啶铜纳米团簇的无标记荧光探针,用于甲基转移酶活性测定。利用末端脱氧核苷酸转移酶催化的高效聚合延伸反应和具有大斯托克斯位移的铜纳米簇代替标记荧光染料,该策略的线性范围从 1 到 300 U mL,检测限为 0.176 U mL。这种经济的方法对 M.SssI 具有特异性,并且还为筛选 DNA 甲基化抑制剂提供了一个方便、高通量的平台,这为未来药物开发和临床癌症诊断的实际应用提供了巨大的潜力。