Paraquat exposure and Sod2 knockdown have dissimilar impacts on the Drosophila melanogaster carbonylated protein proteome

Suresh K. Narayanasamy, David C. Simpson, Ian Martin, Mike Grotewiel, Scott Gronert

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Exposure to Paraquat and RNA interference knockdown of mitochondrial superoxide dismutase (Sod2) are known to result in significant lifespan reduction, locomotor dysfunction, and mitochondrial degeneration in Drosophila melanogaster. Both perturbations increase the flux of the progenitor ROS, superoxide, but the molecular underpinnings of the resulting phenotypes are poorly understood. Improved understanding of such processes could lead to advances in the treatment of numerous age-related disorders. Superoxide toxicity can act through protein carbonylation. Analysis of carbonylated proteins is attractive since carbonyl groups are not present in the 20 canonical amino acids and are amenable to labeling and enrichment strategies. Here, carbonylated proteins were labeled with biotin hydrazide and enriched on streptavidin beads. On-bead digestion was used to release carbonylated protein peptides, with relative abundance ratios versus controls obtained using the iTRAQ MS-based proteomics approach. Western blotting and biotin quantitation assay approaches were also investigated. By both Western blotting and proteomics, Paraquat exposure, but not Sod2 knockdown, resulted in increased carbonylated protein relative abundance. For Paraquat exposure versus control, the median carbonylated protein relative abundance ratio (1.53) determined using MS-based proteomics was in good agreement with that obtained using a commercial biotin quantitation kit (1.36).

Original languageEnglish (US)
Pages (from-to)2566-2577
Number of pages12
JournalProteomics
Volume14
Issue number21-22
DOIs
StatePublished - Nov 1 2014

Keywords

  • Animal proteomics
  • Cytochrome c oxidase
  • Paraquat
  • Protein carbonylation
  • Sod2 knockdown
  • Superoxide

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology

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