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Defining the dopamine transporter proteome by convergent biochemical and in silico analyses.
- Source :
-
Genes, brain, and behavior [Genes Brain Behav] 2007 Feb; Vol. 6 (1), pp. 97-106. - Publication Year :
- 2007
-
Abstract
- Monoamine transporters play a key role in neuronal signaling by mediating reuptake of neurotransmitters from the synapse. The function of the dopamine transporter (DAT), an important member of this family of transporters, is regulated by multiple signaling mechanisms, which result in altered cell surface trafficking of DAT. Protein-protein interactions are likely critical for this mode of transporter regulation. In this study, we identified proteins associated with DAT by immunoprecipitation (IP) followed by mass spectrometry. We identified 20 proteins with diverse cellular functions that can be classified as trafficking proteins, cytoskeletal proteins, ion channels and extracellular matrix-associated proteins. DAT was found to associate with the voltage-gated potassium channel Kv2.1 and synapsin Ib, a protein involved in regulating neurotransmitter release. An in silico analysis provided evidence for common transcriptional regulation of the DAT proteome genes. In summary, this study identified a network of proteins that are primary candidates for functional regulation of the DAT, an important player in mechanisms of mental disorders and drug addiction.
- Subjects :
- Animals
Gene Expression Regulation physiology
Mass Spectrometry
Mice
Neostriatum chemistry
Neostriatum metabolism
Potassium Channels, Voltage-Gated genetics
Potassium Channels, Voltage-Gated metabolism
Protein Transport genetics
Synapsins genetics
Synapsins metabolism
Synaptosomes chemistry
Dopamine Plasma Membrane Transport Proteins metabolism
Gene Expression Regulation genetics
Protein Interaction Mapping
Proteome analysis
Synaptosomes metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1601-1848
- Volume :
- 6
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Genes, brain, and behavior
- Publication Type :
- Academic Journal
- Accession number :
- 16643512
- Full Text :
- https://doi.org/10.1111/j.1601-183X.2006.00236.x