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Cryo-EM structure of SARS-CoV-2 ORF3a in lipid nanodiscs.

Authors :
Kern DM
Sorum B
Mali SS
Hoel CM
Sridharan S
Remis JP
Toso DB
Kotecha A
Bautista DM
Brohawn SG
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.)

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