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 language | English |
|---|---|
| Pages (from-to) | 2374-2389 |
| Number of pages | 15 |
| Journal | Biochimica et Biophysica Acta - Biomembranes |
| Volume | 1808 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - Oct 2011 |
Keywords
- Cluster
- Electron microscopy
- MAGUK
- Potassium channel
- Small angle X-ray scattering