Neurotransmitters Drive Combinatorial Multistate Postsynaptic Density Networks

被引:104
作者
Coba, Marcelo P. [1 ]
Pocklington, Andrew J. [2 ]
Collins, Mark O. [3 ]
Kopanitsa, Maksym V. [1 ]
Uren, Rachel T. [1 ]
Swamy, Sajani [3 ]
Croning, Mike D. R. [1 ]
Choudhary, Jyoti S. [3 ]
Grant, Seth G. N. [1 ]
机构
[1] Wellcome Trust Sanger Inst, Genes Cognit, Hinxton CB10 1SA, Cambs, England
[2] Univ Edinburgh, Div Informat, Inst Adapt & Neural Computat, Edinburgh EH1 2QL, Midlothian, Scotland
[3] Wellcome Trust Sanger Inst, Prote Mass Spectrometry, Hinxton CB10 1SA, Cambs, England
关键词
LONG-TERM POTENTIATION; PROTEIN-KINASE-II; PHOSPHORYLATION SITES; PROTEOMIC ANALYSIS; REGULATORY PHOSPHORYLATION; GLUTAMATE RECEPTORS; SYNAPTIC PLASTICITY; SIGNALING NETWORKS; MEMORY STORAGE; GLUR1; SUBUNIT;
D O I
10.1126/scisignal.2000102
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian postsynaptic density (PSD) comprises a complex collection of similar to 1100 proteins. Despite extensive knowledge of individual proteins, the overall organization of the PSD is poorly understood. Here, we define maps of molecular circuitry within the PSD based on phosphorylation of postsynaptic proteins. Activation of a single neurotransmitter receptor, the N-methyl-D-aspartate receptor (NMDAR), changed the phosphorylation status of 127 proteins. Stimulation of ionotropic and metabotropic glutamate receptors and dopamine receptors activated overlapping networks with distinct combinatorial phosphorylation signatures. Using peptide array technology, we identified specific phosphorylation motifs and switching mechanisms responsible for the integration of neurotransmitter receptor pathways and their coordination of multiple substrates in these networks. These combinatorial networks confer high information-processing capacity and functional diversity on synapses, and their elucidation may provide new insights into disease mechanisms and new opportunities for drug discovery.
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页数:11
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