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Neuron. 2005 Sep 15;47(6):845-57.

The synaptic localization of NR2B-containing NMDA receptors is controlled by interactions with PDZ proteins and AP-2.

Author information

1
Laboratory of Neurochemistry, National Institute on Deafness and Other Communication Disorders, Room 4148/Bldg. 50, National Institutes of Health, Bethesda Maryland 20892, USA. prybylow@nidcd.nih.gov

Abstract

The NMDA receptor (NMDAR) is a component of excitatory synapses and a key participant in synaptic plasticity. We investigated the role of two domains in the C terminus of the NR2B subunit--the PDZ binding domain and the clathrin adaptor protein (AP-2) binding motif--in the synaptic localization of NMDA receptors. NR2B subunits lacking functional PDZ binding are excluded from the synapse. Mutations in the AP-2 binding motif, YEKL, significantly increase the number of synaptic receptors and allow the synaptic localization of NR2B subunits lacking PDZ binding. Peptides corresponding to YEKL increase the synaptic response within minutes. In contrast, the NR2A subunit localizes to the synapse in the absence of PDZ binding and is not altered by mutations in its motif corresponding to YEKL of NR2B. This study identifies a dynamic regulation of synaptic NR2B-containing NMDARs through PDZ protein-mediated stabilization and AP-2-mediated internalization that is modulated by phosphorylation by Fyn kinase.

PMID:
16157279
PMCID:
PMC1350965
DOI:
10.1016/j.neuron.2005.08.016
[Indexed for MEDLINE]
Free PMC Article

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