Skip to main navigation Skip to search Skip to main content

Redox proteomics identification of oxidatively modified brain proteins in inherited Alzheimer's disease: An initial assessment

  • D. Allan Butterfield
  • , Anastazija Gnjec
  • , H. Fai Poon
  • , Alessandra Castegna
  • , William M. Pierce
  • , Jon B. Klein
  • , Ralph N. Martins

Research output: Contribution to journal › Article › peer-review

117 Scopus citations

Abstract

Objective: To identify oxidatively modified proteins in brains of persons with inherited Alzheimer's disease. Methods: Redox proteomics was used to identify oxidatively modified brain proteins in persons with mutations in the genes for presenilin-1 (PS-1). Results: An initial redox proteomics assessment of oxidatively modified proteins from brains of individuals with PS-1 mutations was performed. These PS1 mutations, Q222H and M233T, are completely penetrant causing early-onset familial AD as previously reported in these Australian families. We show that oxidative modifications of ubiquitin carboxyl-terminal hydrolase L1 (UCH-L1), γ-enolase, actin, and dimethylarginine dimethylaminohydrolase 1 (DMDMAH-1) are present in the brain of familial AD subjects. Conclusions: These initial results suggest that oxidatively modified proteins are important common features in both familial and sporadic AD.

Original languageEnglish
Pages (from-to)391-397
Number of pages7
JournalJournal of Alzheimer's Disease
Volume10
Issue number4
DOIs
StatePublished - 2006

Funding

FundersFunder number
National Institute on AgingP01AG010836

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Familial Alzheimer's disease
    • Oxidatively modified brain proteins
    • Redox proteomics

    ASJC Scopus subject areas

    • General Neuroscience
    • Clinical Psychology
    • Geriatrics and Gerontology
    • Psychiatry and Mental health

    Fingerprint

    Dive into the research topics of 'Redox proteomics identification of oxidatively modified brain proteins in inherited Alzheimer's disease: An initial assessment'. Together they form a unique fingerprint.

    Cite this