Literature DB >> 22744909

Dopaminergic modulation of the hippocampal neuropil proteome identified by bioorthogonal noncanonical amino acid tagging (BONCAT).

Jennifer J L Hodas1, Anne Nehring, Nicole Höche, Michael J Sweredoski, Rainer Pielot, Sonja Hess, David A Tirrell, Daniela C Dieterich, Erin M Schuman.   

Abstract

Local protein synthesis and its activity-dependent modulation via dopamine receptor stimulation play an important role in synaptic plasticity - allowing synapses to respond dynamically to changes in their activity patterns. We describe here the metabolic labeling, enrichment, and MS-based identification of candidate proteins specifically translated in intact hippocampal neuropil sections upon treatment with the selective D1/D5 receptor agonist SKF81297. Using the noncanonical amino acid azidohomoalanine and click chemistry, we identified over 300 newly synthesized proteins specific to dendrites and axons. Candidates specific for the SKF81297-treated samples were predominantly involved in protein synthesis and synapse-specific functions. Furthermore, we demonstrate a dendrite-specific increase in proteins synthesis upon application of SKF81297. This study provides the first snapshot in the dynamics of the dopaminergic hippocampal neuropil proteome.
© 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2012        PMID: 22744909      PMCID: PMC3752339          DOI: 10.1002/pmic.201200112

Source DB:  PubMed          Journal:  Proteomics        ISSN: 1615-9853            Impact factor:   3.984


  62 in total

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2.  Ran-binding protein 5 (RanBP5) is related to the nuclear transport factor importin-beta but interacts differently with RanBP1.

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Review 5.  The dopaminergic mesencephalic projections to the hippocampal formation in the rat.

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Authors:  A James Link; Mandy K S Vink; David A Tirrell
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  28 in total

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4.  Quantitative, time-resolved proteomic analysis by combining bioorthogonal noncanonical amino acid tagging and pulsed stable isotope labeling by amino acids in cell culture.

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9.  A genetically encoded and gate for cell-targeted metabolic labeling of proteins.

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