Self-directed assembly and clustering of the cytoplasmic domains of inwardly rectifying Kir2.1 potassium channels on association with PSD-95

Svetlana Fomina, Tina D. Howard, Olivia K. Sleator, Marina Golovanova, Liam O'Ryan, Mark L. Leyland, J. Günter Grossmann, Richard F. Collins, Stephen M. Prince

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The interaction of the extra-membranous domain of tetrameric inwardly rectifying Kir2.1 ion channels (Kir2.1NC4) with the membrane associated guanylate kinase protein PSD-95 has been studied using Transmission Electron Microscopy in negative stain. Three types of complexes were observed in electron micrographs corresponding to a 1:1 complex, a large self-enclosed tetrad complex and extended chains of linked channel domains. Using models derived from small angle X-ray scattering experiments in which high resolution structures from X-ray crystallographic and Nuclear Magnetic Resonance studies are positioned, the envelopes from single particle analysis can be resolved as a Kir2.1NC4:PSD-95 complex and a tetrad of this unit (Kir2.1NC 4:PSD-95)4. The tetrad complex shows the close association of the Kir2.1 cytoplasmic domains and the influence of PSD-95 mediated self-assembly on the clustering of these channels. © 2011 Elsevier B.V. All rights reserved.
    Original languageEnglish
    Pages (from-to)2374-2389
    Number of pages15
    JournalBiochimica et Biophysica Acta - Biomembranes
    Volume1808
    Issue number10
    DOIs
    Publication statusPublished - Oct 2011

    Keywords

    • Cluster
    • Electron microscopy
    • MAGUK
    • Potassium channel
    • Small angle X-ray scattering

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