A graphene oxide-based fluorescence assay for the sensitive detection of DNA exonuclease enzymatic activity. Issue 21 (25th September 2019)

• Record Type: Journal Article
• Authors: Liu, Xiao; Wu, Yingfen; Wu, Xu; Zhao, Julia Xiaojun
• Is Part Of: Analyst. Volume 144:Issue 21(2019)
• Page Start: 6231
• Page End: 6239
• Publication Date: 2019-09-25
• Subjects: Chemistry, Analytic -- Periodicals; 543
• DOI: 10.1039/c9an01283d
• Languages: English
• ISSNs: 0003-2654

Abstract

Abstract : A simple and ultra-sensitive fluorescent sensor was developed to detect the enzymatic activity of Exo III with a limit of detection of 0.001 U mL −1 . Abstract : The 3′–5′ exonuclease enzyme plays a dominant role in multiple pivotal physiological activities, such as DNA replication and repair processes. In this study, we designed a sensitive graphene oxide (GO)-based probe for the detection of exonuclease enzymatic activity. In the absence of Exo III, the strong π–π interaction between the fluorophore-tagged DNA and GO causes the efficient fluorescence quenching via a fluorescence resonance energy transfer (FRET). In contrast, in the presence of Exo III, the fluorophore-tagged 3′-hydroxyl termini of the DNA probe was digested by Exo III to set the fluorophore free from adsorption when GO was introduced, causing an inefficient fluorescence quenching. As a result, the fluorescence intensity of the sensor was found to be proportional to the concentration of Exo III; towards the detection of Exo III, this simple GO-based probe demonstrated a highly sensitive and selective linear response in the low detection range from 0.01 U mL −1 to 0.5 U mL −1 and with the limit of detection (LOD) of 0.001 U mL −1 . Compared with other fluorescent probes, this assay exhibited superior sensitivity and selectivity in both buffer and fetal bovine serum samples, in addition to being cost effective and having a simple setup.