Hu Yufang, Zhang Qingqing, Xu Lihua, Wang Jiao, Rao Jiajia, Guo Zhiyong, Wang Sui
Faculty of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhèjiāng, 315211, China.
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan, 410082, China.
Anal Bioanal Chem. 2017 Nov;409(28):6677-6688. doi: 10.1007/s00216-017-0623-0. Epub 2017 Sep 29.
Electrochemical methods allow fast and inexpensive analysis of enzymatic activity. Here, a simple and yet efficient "signal-on" electrochemical assay for sensitive, label-free detection of DNA-related enzyme activity was established on the basis of terminal deoxynucleotidyl transferase (TdT)-mediated extension strategy. TdT, which is a template-independent DNA polymerase, can catalyze the sequential addition of deoxythymidine triphosphate (dTTP) at the 3'-OH terminus of single-stranded DNA (ssDNA); then, the TdT-yield T-rich DNA nanowires can be employed as the synthetic template of copper nanoclusters (CuNCs). Grown DNA nanowires-templated CuNCs (noted as DNA-CuNCs) were attached onto graphene oxide (GO) surface and exhibited unique electrocatalytic activity to HO reduction. Under optimal conditions, the proposed biosensor was utilized for quantitatively monitoring TdT activity, with the observed LOD of 0.1 U/mL. It also displayed high selectivity to TdT with excellent stability, and offered a facile, convenient electrochemical method for TdT-relevant inhibitors screening. Moreover, the proposed sensor was successfully used for BamHI activity detection, in which a new 3'-OH terminal was exposed by the digestion of a phosphate group. Ultimately, it has good prospects in DNA-related enzyme-based biochemical studies, disease diagnosis, and drug discovery. Graphical Abstract Extraordinary TdT-generated DNA-CuNCs are synthesized and act as a novel electrochemical sensing platform for sensitive detection of TdT and BamHI activity in biological environments.
电化学方法能够对酶活性进行快速且低成本的分析。在此,基于末端脱氧核苷酸转移酶(TdT)介导的延伸策略,建立了一种简单而高效的“信号开启”电化学分析方法,用于灵敏、无标记地检测与DNA相关的酶活性。TdT是一种不依赖模板的DNA聚合酶,它能催化在单链DNA(ssDNA)的3'-OH末端依次添加三磷酸脱氧胸苷(dTTP);然后,TdT产生的富含T的DNA纳米线可作为铜纳米簇(CuNCs)的合成模板。以生长的DNA纳米线为模板的CuNCs(记为DNA-CuNCs)附着在氧化石墨烯(GO)表面,并对HO还原表现出独特的电催化活性。在最佳条件下,所提出的生物传感器用于定量监测TdT活性,观察到的检测限为0.1 U/mL。它对TdT还表现出高选择性和出色的稳定性,并为筛选与TdT相关的抑制剂提供了一种简便的电化学方法。此外,所提出的传感器成功用于BamHI活性检测,其中通过磷酸基团的消化暴露了一个新的3'-OH末端。最终,它在基于DNA相关酶的生化研究、疾病诊断和药物发现方面具有良好的前景。图形摘要 合成了由TdT产生的非凡DNA-CuNCs,并将其作为一种新型电化学传感平台,用于在生物环境中灵敏检测TdT和BamHI活性。