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Proteomic analysis of NMDA receptor-adhesion protein signaling complexes.

TitleProteomic analysis of NMDA receptor-adhesion protein signaling complexes.
Publication TypeJournal Article
Year of Publication2000
AuthorsHusi H, Ward MA, Choudhary JS, Blackstock WP, Grant SG
JournalNat Neurosci
Volume3
Issue7
Pagination661-9
Date Published2000 Jul
ISSN1097-6256
KeywordsAnimals, Brain, Cadherins, Cytoskeletal Proteins, Humans, Mass Spectrometry, Mice, Nerve Tissue Proteins, Neurotransmitter Agents, Protein Kinases, Receptors, N-Methyl-D-Aspartate, Signal Transduction
Abstract

N-methyl-d-aspartate receptors (NMDAR) mediate long-lasting changes in synapse strength via downstream signaling pathways. We report proteomic characterization with mass spectrometry and immunoblotting of NMDAR multiprotein complexes (NRC) isolated from mouse brain. The NRC comprised 77 proteins organized into receptor, adaptor, signaling, cytoskeletal and novel proteins, of which 30 are implicated from binding studies and another 19 participate in NMDAR signaling. NMDAR and metabotropic glutamate receptor subtypes were linked to cadherins and L1 cell-adhesion molecules in complexes lacking AMPA receptors. These neurotransmitter-adhesion receptor complexes were bound to kinases, phosphatases, GTPase-activating proteins and Ras with effectors including MAPK pathway components. Several proteins were encoded by activity-dependent genes. Genetic or pharmacological interference with 15 NRC proteins impairs learning and with 22 proteins alters synaptic plasticity in rodents. Mutations in three human genes (NF1, Rsk-2, L1) are associated with learning impairments, indicating the NRC also participates in human cognition.

DOI10.1038/76615
Alternate JournalNat. Neurosci.
PubMed ID10862698