Department of Chemistry, Soonchunhyang University, Asan 31538, Republic of Korea.
Biosensors (Basel). 2024 Jan 30;14(2):73. doi: 10.3390/bios14020073.
An electrochemically reduced graphene oxide (ERGO) electrode-based electrochemical assay was developed for rapid, sensitive, and straightforward analysis of both activity and inhibition of the endonuclease EcoRV. The procedure uses a DNA substrate designed for EcoRV, featuring a double-stranded DNA (dsDNA) region labeled with methylene blue (MB) and a single-stranded DNA (ssDNA) region immobilized on the ERGO surface. The ERGO electrode, immobilized with the DNA substrate, was subsequently exposed to a sample containing EcoRV. Upon enzymatic hydrolysis, the cleaved dsDNA fragments were detached from the ERGO surface, leading to a decrease in the MB concentration near the electrode. This diminished the electron transfer efficiency for MB reduction, resulting in a decreased reduction current. This assay demonstrates excellent specificity and high sensitivity, with a limit of detection (LOD) of 9.5 × 10 U mL. Importantly, it can also measure EcoRV activity in the presence of aurintricarboxylic acid, a known inhibitor, highlighting its potential for drug discovery and clinical diagnostic applications.
一种基于电化学还原氧化石墨烯(ERGO)电极的电化学分析方法被开发出来,用于快速、灵敏、直接地分析内切酶 EcoRV 的活性和抑制作用。该方法使用了一种专为 EcoRV 设计的 DNA 底物,其具有带有亚甲基蓝(MB)标记的双链 DNA(dsDNA)区域和固定在 ERGO 表面的单链 DNA(ssDNA)区域。固定有 DNA 底物的 ERGO 电极随后暴露于含有 EcoRV 的样品中。在酶水解后,dsDNA 片段从 ERGO 表面脱离,导致电极附近 MB 浓度降低。这降低了 MB 还原的电子转移效率,导致还原电流减少。该分析方法表现出优异的特异性和高灵敏度,检测限(LOD)为 9.5×10 U mL。重要的是,它还可以在存在已知抑制剂金精三羧酸的情况下测量 EcoRV 活性,这突出了它在药物发现和临床诊断应用方面的潜力。