A unique residue in rab3c determines the interaction with novel binding protein Zwint-1
Exocytic events are tightly regulated cellular processes in which rab GTPases and their interacting proteins perform an important function. We set out to identify new binding partners of rab3, which mediates regulated secretion events in specialized cells. We discovered Zwint-1 as a rab3 specific binding protein that bound preferentially to rab3c. The interaction depends on a critical residue in rab3c that determines the binding efficiency of Zwint-1, which is immaterial for interaction with rabphilin3a. Rab3c and Zwint-1 are expressed highly in brain and colocalized extensively in primary hippocampal neurons. We also found that SNAP25 bound to the same region in Zwint-1 as rab3c, suggesting a new role for the kinetochore protein Zwint-1 in presynaptic events that are regulated by rab3 and SNAP25.
|Keywords||Rab3, Rabphilin3a, SNAP25, Zwint-1|
|Persistent URL||dx.doi.org/10.1016/j.febslet.2008.07.012, hdl.handle.net/1765/28747|
|Journal||F E B S Letters|
van Vlijmen, T, Vleugel, M, Evers, M, Mohammed, S, Wulf, P, Heck, A.J.R, … van der Sluijs, P. (2008). A unique residue in rab3c determines the interaction with novel binding protein Zwint-1. F E B S Letters, 582(19), 2838–2842. doi:10.1016/j.febslet.2008.07.012