Mamma Mia, P-glycoprotein binds again

Richard Callaghan*, Ingrid C. Gelissen, Anthony M. George, Anika M.S. Hartz

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    9 Citations (Scopus)

    Abstract

    The levels of amyloid peptides in the brain are regulated by a clearance pathway from neurons to the blood–brain barrier. The first step is thought to involve diffusion from the plasma membrane to the interstitium. However, amyloid peptides are hydrophobic and avidly intercalate within membranes. The ABC transporter P-glycoprotein is implicated in the clearance of amyloid peptides across the blood–brain, but its role at neurons is undetermined. We here propose that P-glycoprotein mediates 'exit' of amyloid peptides from neurons. Indeed, amyloid peptides have physicochemical similarities to substrates of P-glycoprotein, but their larger size represents a conundrum. This review probes the plausibility of a mechanism for amyloid peptide transport by P-glycoprotein exploiting evolving biochemical and structural models.

    Original languageEnglish
    Pages (from-to)4076-4084
    Number of pages9
    JournalFEBS Letters
    Volume594
    Issue number23
    DOIs
    Publication statusPublished - Dec 2020

    Fingerprint

    Dive into the research topics of 'Mamma Mia, P-glycoprotein binds again'. Together they form a unique fingerprint.

    Cite this