Published in

Wiley, FEBS Letters, 21(586), p. 3813-3818, 2012

DOI: 10.1016/j.febslet.2012.09.022

Links

Tools

Export citation

Search in Google Scholar

Cdk5-mediated phosphorylation of CRMP-2 enhances its interaction with CaV2.2

Journal article published in 2012 by Joel M. Brittain, Yuying Wang, Omotore Eruvwetere, Rajesh Khanna ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

Full text: Download

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

The axon/dendrite specification collapsin response mediator protein-2 (CRMP-2) bidirectionally regulates N-type voltage-gated Ca(2+) channels (CaV2.2). But how cyclin dependent kinase 5 (Cdk5)-mediated phosphorylation of CRMP-2 affects its interaction/regulation with CaV2.2 is unknown. CRMP-2-mediated enhancement of currents via CaV2.2 was not observed with a Cdk5 phospho-null CRMP-2-S522A mutant or in cells expressing an inactive Cdk5. Concomitant knockdown of endogenous CRMP2 and overexpression of CRMP2-S522A mutant refractory to knockdown phenocopied the reduction in Ca(2+) influx while the Rho kinase CRMP2-T555A mutant was ineffective. Cdk5-phosphorylated CRMP-2 had increased association with CaV2.2. These results identify an important role for Cdk5 in CRMP2-mediated CaV2.2 regulation. STRUCTURED SUMMARY OF PROTEIN INTERACTIONS: Gsk3bphosphorylatesCrmp2by phosphatase assay (View interaction) Crmp2physically interacts with Cav2.2 by anti tag coimmunoprecipitation (View interaction).