Fluorescence detection of glutathione reductase activity based on deoxyribonucleic acid-templated silver nanoclusters

• DNA-Ag nanocluster-based glutathione reductase sensor is reported for the first time.
• It is based on fluorescence enhancement in the presence of glutathione reductase.
• The present sensor exhibits good selectivity toward glutathione reductase.

Fluorescent silver nanoclusters stabilized by DNA (DNA-AgNCs) exhibit distinct response rates to thiol and disulfide. Glutathione reductase can catalyze the reduction of the oxidized glutathione (GSSG) quickly to reduced glutathione (GSH) in the presence of β-nicotinamide adenine dinucleotide 2′-phosphate reduced tetrasodium salt hydrate (NADPH). Consequently, DNA-AgNCs can serve as a new fluorescent platform for assaying the glutathione reductase (GR) activity. This newly proposed assay has a high sensitivity and a good selectivity toward GR. The GR activity can be detected in the range of 0.2–2.0 mU mL−1 with a minimum detectable concentration of 0.2 mU mL−1. Pepsin, lysozyme, trypsin, avidin, thrombin, myoglobin, and BSA have little effect on the fluorescence intensity of DNA-AgNCs. The GR activity assay is successfully used to monitor the inhibition of GR activity by a typical inhibitor 1,3-bis(2-chloroethyl)-1-nitrosourea.

Fluorescent silver nanoclusters stabilized by DNA have been used to develop a fluorescent platform for assaying glutathione reductase activity for the first time.Figure optionsDownload as PowerPoint slide