Structure of the complete, membrane-assembled COPII coat reveals a complex interaction network.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 33795673.
- Also identified by DOI 10.1038/s41467-021-22110-6 and PMC identifier 8016994.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
COPII mediates Endoplasmic Reticulum to Golgi trafficking of thousands of cargoes. Five essential proteins assemble into a two-layer architecture, with the inner layer thought to regulate coat assembly and cargo recruitment, and the outer coat forming cages assumed to scaffold membrane curvature. Here we visualise the complete, membrane-assembled COPII coat by cryo-electron tomography and subtomogram averaging, revealing the full network of interactions within and between coat layers. We demonstrate the physiological importance of these interactions using genetic and biochemical approaches. Mutagenesis reveals that the inner coat alone can provide membrane remodelling function, with organisational input from the outer coat. These functional roles for the inner and outer coats significantly move away from the current paradigm, which posits membrane curvature derives primarily from the outer coat. We suggest these interactions collectively contribute to coat organisation and membrane curvature, providing a structural framework to understand regulatory mechanisms of COPII trafficking and secretion.
Medical subject headings
- COP-Coated Vesicles
- Endoplasmic Reticulum
- Golgi Apparatus
- Protein Interaction Maps
- Vesicular Transport Proteins