Electrochemical DNA Cleavage Sensing for EcoRV Activity and Inhibition with an ERGO Electrode.
Da Eun OhHyun Beom KimTae Hyun KimPublished in: Biosensors (2024)
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 -3 U mL -1 . 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.
Keyphrases
- circulating tumor
- cell free
- gold nanoparticles
- single molecule
- reduced graphene oxide
- electron transfer
- drug discovery
- nucleic acid
- ionic liquid
- carbon nanotubes
- high throughput
- label free
- loop mediated isothermal amplification
- binding protein
- molecularly imprinted
- solid state
- nitric oxide
- dna repair
- pet imaging
- dna binding
- high resolution
- mass spectrometry
- structural basis