Proteome map of the human hippocampus

Paul F. Edgar, Judith E. Douglas, Catriona Knight, Garth J S Cooper, Richard L M Faull, Robb Kydd

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The proteins expressed by a genome have been termed the proteome. By comparing the proteome of a disease-affected tissue with the proteome of an unaffected tissue it is possible to identify proteins that play a role in a disease process. The hippocampus is involved in the processing of short-term memory and is affected in Alzheimer's disease. Any comparative proteome analysis that can identify proteins important in a disease affecting the hippocampus requires the characterization of the normal hippocampal proteome. Therefore, we homogenised normal hippocampal tissue and separated the proteins by two-dimensional polyacrylamide gel electrophoresis (2DE). Seventy-two unique protein spots were collected from Coomassie blue-stained 2DE gels and subjected to in-gel digestion with trypsin, reversed-phase high-pressure liquid chromatography peptide separation, and N-terminal protein sequencing. Sufficient protein sequence was obtained to successfully characterize 66 of the 72 protein spots chosen (92%). Three of the 66 proteins were not present in any database (4.5%). The characterized proteins comprised two dominant functional groups, i.e., enzymes involved in intermediary cellular metabolism (40%), and proteins associated with the cytoskeleton (15%). The identity, molecular mass, isoelectric point, and relative concentration of the characterized proteins are described and constitute a partial proteome map of the normal human hippocampus.
    Original languageEnglish
    Pages (from-to)644-650
    Number of pages6
    JournalHippocampus
    Volume9
    Issue number6
    DOIs
    Publication statusPublished - 1999

    Keywords

    • Brain mapping
    • Database
    • N-terminal protein sequencing
    • Protein expression
    • Two-dimensional polyacrylamide gel electrophoresis

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