Striatal-enriched protein-tyrosine phosphatase (STEP) regulates Pyk2 kinase activity

Jian Xu, Pradeep Kurup, Jason A. Bartos, Tommaso Patriarchi, Johannes W. Hell, Paul J. Lombroso

Research output: Contribution to journalArticlepeer-review

67 Scopus citations


Proline-rich tyrosine kinase 2 (Pyk2) is a member of the focal adhesion kinase family and is highly expressed in brain and hematopoietic cells. Pyk2 plays diverse functions in cells, including the regulation of cell adhesion, migration, and cytoskeletal reorganization. In the brain, it is involved in the induction of long term potentiation through regulation of N-methyl-D-aspartate receptor trafficking. This occurs through the phosphorylation and activation of Src family tyrosine kinase members, such as Fyn, that phosphorylate GluN2B at Tyr 1472. Phosphorylation at this site leads to exocytosis of GluN1-GluN2B receptors to synaptic membranes. Pyk2 activity is modulated by phosphorylation at several critical tyrosine sites, including Tyr 402. In this study, we report that Pyk2 is a substrate of striatal-enriched protein-tyrosine phosphatase (STEP). STEP binds to and dephosphorylates Pyk2 at Tyr 402. STEP KO mice showed enhanced phosphorylation of Pyk2 at Tyr 402 and of the Pyk2 substrates paxillin and ASAP1. Functional studies indicated that STEP opposes Pyk2 activation after KCl depolarization of cortical slices and blocks Pyk2 translocation to postsynaptic densities, a key step required for Pyk2 activation and function. This is the first study to identify Pyk2 as a substrate for STEP.

Original languageEnglish (US)
Pages (from-to)20942-20956
Number of pages15
JournalJournal of Biological Chemistry
Issue number25
StatePublished - Jun 15 2012


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