How calcium makes endocytic receptors attractive

Christian B F Andersen, Søren K Moestrup

    Research output: Contribution to journalJournal articleResearchpeer-review


    Nutrients, biological waste-products, toxins, pathogens, and other ligands for endocytosis are typically captured by multidomain receptors with multiligand specificity. Upon internalization, the receptor-ligand complex segregates, followed by lysosomal degradation of the ligand and recycling of the receptor. Endosomal acidification and calcium efflux lead to the essential ligand-receptor affinity switch and separation. Recent data, including crystal structures of receptor-ligand complexes, now reveal how calcium, in different types of domain scaffolds, functions in a common way as a removable 'lynchpin' that stabilizes favorable positioning of ligand-attractive receptor residues. In addition to explaining how calcium depletion can cause ligand-receptor dissociation, the new data add further insight into how acidification contributes to dissociation through structural changes that affect the receptor calcium sites.

    Original languageEnglish
    JournalTrends in Biochemical Sciences
    Issue number2
    Pages (from-to)82-90
    Publication statusPublished - 1. Feb 2014


    • Animals
    • Biological Transport
    • Calcium
    • Calcium Signaling
    • Endocytosis
    • Endosomes
    • Eukaryotic Cells
    • Gene Expression Regulation
    • Humans
    • Hydrogen-Ion Concentration
    • Ligands
    • Models, Molecular
    • Protein Binding
    • Protein Structure, Tertiary
    • Receptors, Cell Surface
    • Scavenger receptor
    • EGF-like
    • LDL receptor
    • CUB
    • C-type lectin


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