Monitoring γ-glutamyl transpeptidase activity and evaluating its inhibitors by a water-soluble near-infrared fluorescent probe
- Li, L., Shi, W., Wu, X., Gong, Q., Li, X., Ma, H.
- Biosensors & bioelectronics 81: 395-400 (Journal)
- Registered Authors
- Li, Xiaohui
- Inhibitors, Near-infrared fluorescent probe, Water-soluble fluorescent probe, γ-Glutamyl transpeptidase
- MeSH Terms
- Enzyme Assays/methods*
- Enzyme Inhibitors/pharmacology
- Fluorescent Dyes/chemistry*
- Infrared Rays
- Optical Imaging/methods
- Spectrometry, Fluorescence/methods*
- Zebrafish Proteins/analysis
- Zebrafish Proteins/antagonists & inhibitors
- Zebrafish Proteins/metabolism
- gamma-Glutamyltransferase/antagonists & inhibitors*
- 26995285 Full text @ Biosens. Bioelectron.
Li, L., Shi, W., Wu, X., Gong, Q., Li, X., Ma, H. (2016) Monitoring γ-glutamyl transpeptidase activity and evaluating its inhibitors by a water-soluble near-infrared fluorescent probe. Biosensors & bioelectronics. 81:395-400.
The first near-infrared fluorescent probe with excellent water-solubility for γ-glutamyl transpeptidase (GGT) has been developed by combining glutathione (GSH) as a recognition unit with a near-infrared hemicyanine fluorophore through an acrylyl linker. The probe exhibits a highly selective and sensitive fluorescent off-on response to GGT with a detection limit of 0.50U/L, and the response mechanism is based on the enzyme-catalyzed cleavage of the γ-glutamyl bond of GSH, followed by the spontaneous intramolecular cyclization and the release of the fluorophore. Notably, the probe has been used to image GGT in zebrafish and evaluate the inhibition ability of three common inhibitors of GGT both in vitro and in vivo, revealing that their inhibition efficiencies are acivicin >6-diazo-5-oxo-L-norleucine >L-serine-borate complex, and their corresponding IC50 values are 0.11±0.01mM, 0.34±0.04mM and 2.06±0.24mM, respectively. The proposed probe is simple, and may have great potential for screening GGT inhibitors.
Genes / Markers
Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Engineered Foreign Genes
Errata and Notes