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Updated: Mar 30, 2026

Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein
Published on: June 30, 2019
Quantitative analysis of protein orientation in membrane environments by kinase activity
Wen Xiong1, Chunshan Quan1, Xuning Zhang2
1Department of Life Science, Dalian Nationalities University, Economical and Technological Development Zone, Dalian 116600, China; Key Laboratory of Biotechnology and Resource Utilization, State Ethnic Affairs Commission and Ministry of Education, Dalian Nationalities University, Economical and Technological Development Zone, Dalian 116600, China.
Abstract:
AgrC is an integral membrane receptor protein with histidine kinase activity in the accessory gene regulator (agr) quorum-sensing system of Staphylococcus aureus. In this study, proteoliposomes were used as a model to investigate AgrC orientation. Many approaches have been described to determine membrane protein orientation, but they are often complicated and time consuming. In this study, AgrC orientation in liposomes was determined by thiol-reactive reagent labeling and a kinase activity assay. Our results suggest use of a kinase activity assay could get an accurate percentage of functional protein orientation and only cost nearly one-sixth of the time compared with the method based on thiol-reactive reagent labeling. We present an effective and rapid method for determining the orientation of membrane protein kinases like AgrC.

