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Subcellular proteomics of dopamine neurons in the mouse brain

Output Details

Preprint June 9, 2021

Published January 31, 2022

Dopaminergic neurons modulate neural circuits and behaviors via dopamine release from expansive, long range axonal projections. The elaborate cytoarchitecture of these neurons is embedded within complex brain tissue, making it difficult to access the neuronal proteome using conventional methods. Here, we demonstrate APEX2 proximity labeling within genetically targeted neurons in the mouse brain, enabling subcellular proteomics with cell type-specificity. By combining APEX2 biotinylation with mass spectrometry, we mapped the somatodendritic and axonal proteomes of midbrain dopaminergic neurons. Our dataset reveals the proteomic architecture underlying proteostasis, axonal metabolism, and neurotransmission in these neurons. We find a significant enrichment of proteins encoded by Parkinson's disease-linked genes in striatal dopaminergic axons, including proteins with previously undescribed axonal localization. These proteomic datasets provide a resource for neuronal cell biology, and this approach can be readily adapted for study of other neural cell types.
Identifier (DOI)
10.7554/eLife.70921
Tags
  • Dopamine
  • Dopaminergic neurons
  • Mouse
  • Neuroscience
  • Original Research
  • Parkinson's disease
  • Proteomics
  • Proximity proteomics

Meet the Authors

  • David Sulzer, PhD

    Lead PI (Core Leadership): Team Sulzer

    Columbia University

  • Peter Sims, PhD

    Key Personnel: Team Sulzer

    Columbia University

  • Ben Hobson, BA

    Key Personnel: Team Sulzer

    Columbia University

  • User avatar fallback logo

    Se Joon Choi

    External Collaborator

  • User avatar fallback logo

    Rajesh K. Soni

    External Collaborator

  • Eugene Mosharov, PhD

    Key Personnel: Team Sulzer

    Columbia University

Aligning Science Across Parkinson's
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