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Compilation of reported protein changes in the brain in Alzheimer’s disease

Author

Listed:
  • Manor Askenazi

    (Biomedical Hosting LLC)

  • Tomas Kavanagh

    (University of Sydney)

  • Geoffrey Pires

    (New York University)

  • Beatrix Ueberheide

    (New York University
    New York University
    New York University)

  • Thomas Wisniewski

    (New York University)

  • Eleanor Drummond

    (University of Sydney
    New York University)

Abstract

Proteomic studies of human Alzheimer’s disease brain tissue have potential to identify protein changes that drive disease, and to identify new drug targets. Here, we analyse 38 published Alzheimer’s disease proteomic studies, generating a map of protein changes in human brain tissue across thirteen brain regions, three disease stages (preclinical Alzheimer’s disease, mild cognitive impairment, advanced Alzheimer’s disease), and proteins enriched in amyloid plaques, neurofibrillary tangles, and cerebral amyloid angiopathy. Our dataset is compiled into a searchable database (NeuroPro). We found 848 proteins were consistently altered in 5 or more studies. Comparison of protein changes in early-stage and advanced Alzheimer’s disease revealed proteins associated with synapse, vesicle, and lysosomal pathways show change early in disease, but widespread changes in mitochondrial associated protein expression change are only seen in advanced Alzheimer’s disease. Protein changes were similar for brain regions considered vulnerable and regions considered resistant. This resource provides insight into Alzheimer’s disease brain protein changes and highlights proteins of interest for further study.

Suggested Citation

  • Manor Askenazi & Tomas Kavanagh & Geoffrey Pires & Beatrix Ueberheide & Thomas Wisniewski & Eleanor Drummond, 2023. "Compilation of reported protein changes in the brain in Alzheimer’s disease," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-40208-x
    DOI: 10.1038/s41467-023-40208-x
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