Adhesion G protein-coupled receptors are a large class of membrane proteins that detect chemical and mechanical stimuli in the body. The GAIN domain plays a central role in the activation of adhesion GPCRs. Until now, research has been limited by the low similarity of the amino acid sequences of different GAIN domains, which has hampered knowledge transfer and comparative analysis. The new numbering system, developed by researchers at Leipzig University, provides a standardised basis for the accurate transfer of research results between different model systems and humans. It is based on the analysis of over 14,000 modelled structures in the GAIN domain, generated using the latest AI techniques.
Peter Hildebrand, Professor of Membrane and Cell Biophysics at Leipzig University, who led the international study, says: "Our new numbering system is an important step forward in GPCR research. It will facilitate basic research and encourage comparative studies. It provides a solid foundation for further research in biochemistry, bioinformatics and structural biology." For example, the newly developed system enables a better understanding of disease-relevant mutations in GAIN domains, providing a deeper insight into their role in diseases such as cancer.
Analysis useful for kidney disease
In the new study, the scientists found that their numbering system also made it possible to analyse and compare the GAIN domains of polycystic kidney disease proteins. This genetic disease causes fluid-filled cysts to form in the kidneys and other organs.
