Ligand-binding sites in human serum amyloid P component

N.H.H. Heegaard, Peter M. H. Heegaard, P. Roepstorff, F.A. Robey

    Research output: Contribution to journalJournal articleResearchpeer-review

    Abstract

    Amyloid P component (AP) is a naturally occurring glycoprotein that is found in serum and basement membranes, AP is also a component of all types of amyloid, including that found in individuals who suffer from Alzheimer's disease and Down's syndrome. Because AP has been found to bind strongly and specifically to certain glycosaminoglycans that are components of amyloid deposits, AP may play an important role in the maintenance of amyloid. In the present work, we isolated and identified two proteolytic fragments of AP that are responsible for its heparin-binding activity. Neither fragment corresponds to published heparin-binding sequences. The structural requirements for activity of the peptides (amino acid residues 27-38 and 192-203 of AP) were examined by means of solid-phase inhibition assays with synthetic peptides, AP-(192-203)-peptide inhibits the Ca2+-dependent binding of AP to heparin with an IC50 of 25 mu M, while the IC50 of AP-(27-38)-peptide and AP-(33-38)-peptide are 10 mu M and 2 mu M, respectively, The understanding of the structure and function of active AP peptides will be useful for development of amyloid-targeted diagnostics and therapeutics.
    Original languageEnglish
    JournalEuropean Journal of Biochemistry
    Volume239
    Issue number3
    Pages (from-to)850-856
    ISSN0014-2956
    DOIs
    Publication statusPublished - 1996

    Keywords

    • peptide
    • amyloid P component
    • heparin
    • Alzheimers capillary electrophoresis

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