
The study determined the kinase activity profiles of human pancreatic beta cells downstream of GLP-1R balanced versus biased agonist stimulations. The results showed that kinomic responses were distinct for acute versus sustained GLP-1R agonist exposure, with individual responses associated with agonists presenting specific bias profiles. The study suggests that differentially biased exendin-phe1 and exendin-asp3 can modulate distinct kinase interaction networks, constituting potential targets for further research on biased GLP-1R downstream signalling.
Like
Save
Share