Proteomic identification of dopamine-conjugated proteins from isolated rat brain mitochondria and SH-SY5Y cells

Neurobiol Dis. 2009 Jun;34(3):487-500. doi: 10.1016/j.nbd.2009.03.004. Epub 2009 Mar 28.

Abstract

Dopamine oxidation has been previously demonstrated to cause dysfunction in mitochondrial respiration and membrane permeability, possibly related to covalent modification of critical proteins by the reactive dopamine quinone. However, specific mitochondrial protein targets have not been identified. In this study, we utilized proteomic techniques to identify proteins directly conjugated with (14)C-dopamine from isolated rat brain mitochondria exposed to radiolabeled dopamine quinone (150 microM) and differentiated SH-SY5Y cells treated with (14)C-dopamine (150 microM). We observed a subset of rat brain mitochondrial proteins that were covalently modified by (14)C-dopamine, including chaperonin, ubiquinol-cytochrome c reductase core protein 1, glucose regulated protein 75/mitochondrial HSP70/mortalin, mitofilin, and mitochondrial creatine kinase. We also found the Parkinson's disease associated proteins ubiquitin carboxy-terminal hydrolase L1 and DJ-1 to be covalently modified by dopamine in both brain mitochondrial preparations and SH-SY5Y cells. The susceptibility of the identified proteins to covalent modification by dopamine may carry implications for their role in the vulnerability of dopaminergic neurons in Parkinson's disease pathogenesis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Benzoquinones / pharmacology
  • Brain / drug effects
  • Brain / physiology*
  • Carbon Radioisotopes / pharmacology
  • Cell Line, Tumor
  • Chaperonins / metabolism
  • Creatine Kinase, Mitochondrial Form / metabolism
  • Dopamine / metabolism*
  • Dopamine / pharmacology
  • Electron Transport Complex III / metabolism
  • HSP70 Heat-Shock Proteins / metabolism
  • Humans
  • Microtubule-Associated Proteins / metabolism
  • Mitochondria / drug effects
  • Mitochondria / physiology*
  • Mitochondrial Proteins / metabolism
  • Oxidants / pharmacology
  • Oxidation-Reduction* / drug effects
  • Protein Deglycase DJ-1
  • Rats
  • Ubiquitin Thiolesterase / metabolism

Substances

  • Benzoquinones
  • Carbon Radioisotopes
  • HSP70 Heat-Shock Proteins
  • Microtubule-Associated Proteins
  • Mitochondrial Proteins
  • Oxidants
  • mortalin
  • quinone
  • Creatine Kinase, Mitochondrial Form
  • PARK7 protein, rat
  • Protein Deglycase DJ-1
  • UCHL1 protein, rat
  • Ubiquitin Thiolesterase
  • Chaperonins
  • Electron Transport Complex III
  • Dopamine