Proteome analysis of DNA damage-induced neuronal death using high throughput mass spectrometry

Mark D. Johnson, Li Rong Yu, Thomas P. Conrads, Yoshito Kinoshita, Takuma Uo, Jesse D. Matthews, Sang-Won Lee, Richard D. Smith, Timothy D. Veenstra, Richard S. Morrison

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Isotope-coded affinity tag reagents and high throughput mass spectrometry were used to quantitate changes in the expression of 150 proteins in mouse wild-type (p53+/+) cortical neurons undergoing DNA damage-induced death. Immunological techniques confirmed several of the changes in protein expression, but microarray analysis indicated that many of these changes were not accompanied by altered mRNA expression. Proteome analysis revealed perturbations in mitochondrial function, free radical production, and neuritogenesis that were not observed in p53-deficient neurons. Changes in Tau, cofilin, and other proteins recapitulated abnormalities observed in neurodegenerative states in vivo. Additionally, DNA damage caused a p53-dependent decrease in expression of members of the protein kinase A (PKA) signaling pathway. PKA inhibition promoted death in the absence of DNA damage, revealing a novel mechanism by which endogenous down-regulation of PKA signaling may contribute to p53-dependent neuronal death. These data demonstrate the power of high throughput mass spectrometry for quantitative analysis of the neuronal proteome.

Original languageEnglish
Pages (from-to)26685-26697
Number of pages13
JournalJournal of Biological Chemistry
Volume279
Issue number25
DOIs
Publication statusPublished - 2004 Jun 18
Externally publishedYes

    Fingerprint

ASJC Scopus subject areas

  • Biochemistry

Cite this

Johnson, M. D., Yu, L. R., Conrads, T. P., Kinoshita, Y., Uo, T., Matthews, J. D., Lee, S-W., Smith, R. D., Veenstra, T. D., & Morrison, R. S. (2004). Proteome analysis of DNA damage-induced neuronal death using high throughput mass spectrometry. Journal of Biological Chemistry, 279(25), 26685-26697. https://doi.org/10.1074/jbc.M401274200