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Cryo-EM structure of SARS-CoV-2 ORF3a in lipid nanodiscs.
- Source :
-
Nature structural & molecular biology [Nat Struct Mol Biol] 2021 Jul; Vol. 28 (7), pp. 573-582. Date of Electronic Publication: 2021 Jun 22. - Publication Year :
- 2021
-
Abstract
- SARS-CoV-2 ORF3a is a putative viral ion channel implicated in autophagy inhibition, inflammasome activation and apoptosis. 3a protein and anti-3a antibodies are found in infected patient tissues and plasma. Deletion of 3a in SARS-CoV-1 reduces viral titer and morbidity in mice, suggesting it could be an effective target for vaccines or therapeutics. Here, we present structures of SARS-CoV-2 3a determined by cryo-EM to 2.1-Å resolution. 3a adopts a new fold with a polar cavity that opens to the cytosol and membrane through separate water- and lipid-filled openings. Hydrophilic grooves along outer helices could form ion-conduction paths. Using electrophysiology and fluorescent ion imaging of 3a-reconstituted liposomes, we observe Ca <superscript>2+</superscript> -permeable, nonselective cation channel activity, identify mutations that alter ion permeability and discover polycationic inhibitors of 3a activity. 3a-like proteins are found across coronavirus lineages that infect bats and humans, suggesting that 3a-targeted approaches could treat COVID-19 and other coronavirus diseases.<br /> (© 2021. The Author(s), under exclusive licence to Springer Nature America, Inc.)
- Subjects :
- Animals
Calcium metabolism
Chiroptera virology
Coronaviridae
Electrophysiology
Fluorescence
Humans
Ion Transport
Liposomes
Models, Molecular
Open Reading Frames
Optical Imaging
Reproducibility of Results
Sequence Homology
Viral Proteins chemistry
Viral Proteins ultrastructure
Viroporin Proteins antagonists & inhibitors
Cryoelectron Microscopy
Nanostructures chemistry
Nanostructures ultrastructure
SARS-CoV-2 chemistry
SARS-CoV-2 ultrastructure
Viroporin Proteins chemistry
Viroporin Proteins ultrastructure
Subjects
Details
- Language :
- English
- ISSN :
- 1545-9985
- Volume :
- 28
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Nature structural & molecular biology
- Publication Type :
- Academic Journal
- Accession number :
- 34158638
- Full Text :
- https://doi.org/10.1038/s41594-021-00619-0