Related Experiment Video
Updated: Oct 26, 2025

Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein
Published on: June 30, 2019
Generation of a quenched phosphonate activity-based probe for labelling the active KLK7 protease
Evangelos Bisyris1, Eleni Zingkou1, Golfo G Kordopati1
1Department of Pharmacy, School of Health Sciences, University of Patras, Rion-Patras, 265 04, Greece. gdsotiro@upatras.gr.
Abstract:
Kallikrein 7 (KLK7) is a chymotrypsin-like serine protease with established roles in skin diseases like the rare Netherton syndrome, an overdesquamating and inflammatory condition, but also common atopic dermatitis, and a potential drug target for these and possibly other diseases. Nevertheless, tools to determine the active KLK7 enzyme are not available. Here, a mixed alkyl aryl phosphonate quenched activity-based probe that detects the active KLK7 was developed and evaluated in vitro. This KLK7-qABP can potentially be used to monitor KLK7 activity in vivo.

