Csk binding to integrin β3 is regulated by tyrosine and threonine phosphorylation of β3
C-terminal Src kinase (Csk) is crucial for the normal function of platelet integrin αIIbβ3 because it inactivates Src kinase. While the molecular mechanism by which cytoplasmic Csk associates with membrane-bound Src is known in resting platelets, it remains unknown in activated platelets. Using surface plasmon resonance, a kinase assay, and microscale thermophoresis, we discovered that Csk binds directly to phospho-Tyr747 on the β3 tail via its SH2 domain and that this binding fully activates Csk. Moreover, we found that phospho-Thr753 on the β3 tail prevents Csk from binding. Collectively, our findings provide new insight into the regulation of Csk function in activated platelets, suggesting that Tyr747-phosphorylated β3 recruits Csk near active Src, whereas phospho-Thr753 on β3 inhibits this interaction.
Authors
- Esa T. Mikkola
- Carl G. Gahmberg
Institutions
- University of Helsinki (FI)
Publication Details
- Journal
- FEBS Letters
- Published
- 2026-06-26
- DOI
- https://doi.org/10.1002/1873-3468.70401
- Primary Topic
- Platelet Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00