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Inhibition of HECT E3 ligases as potential therapy for COVID-19

Authors :
Giuseppe Novelli
Jing Liu
Michela Biancolella
Tonino Alonzi
Antonio Novelli
J. J. Patten
Dario Cocciadiferro
Emanuele Agolini
Vito Luigi Colona
Barbara Rizzacasa
Rosalinda Giannini
Benedetta Bigio
Delia Goletti
Maria Rosaria Capobianchi
Sandro Grelli
Justin Mann
Trevor D. McKee
Ke Cheng
Fatima Amanat
Florian Krammer
Andrea Guarracino
Gerardo Pepe
Carlo Tomino
Yacine Tandjaoui-Lambiotte
Yurdagul Uzunhan
Sarah Tubiana
Jade Ghosn
COVID Human Genetic Effort
French COVID Cohort Study Group
CoV-Contact Cohort
Luigi D. Notarangelo
Helen C. Su
Laurent Abel
Aurélie Cobat
Gai Elhanan
Joseph J. Grzymski
Andrea Latini
Sachdev S. Sidhu
Suresh Jain
Robert A. Davey
Jean-Laurent Casanova
Wenyi Wei
Pier Paolo Pandolfi
Source :
Cell Death and Disease, Vol 12, Iss 4, Pp 1-18 (2021)
Publication Year :
2021
Publisher :
Nature Publishing Group, 2021.

Abstract

Abstract SARS-CoV-2 is responsible for the ongoing world-wide pandemic which has already taken more than two million lives. Effective treatments are urgently needed. The enzymatic activity of the HECT-E3 ligase family members has been implicated in the cell egression phase of deadly RNA viruses such as Ebola through direct interaction of its VP40 Protein. Here we report that HECT-E3 ligase family members such as NEDD4 and WWP1 interact with and ubiquitylate the SARS-CoV-2 Spike protein. Furthermore, we find that HECT family members are overexpressed in primary samples derived from COVID-19 infected patients and COVID-19 mouse models. Importantly, rare germline activating variants in the NEDD4 and WWP1 genes are associated with severe COVID-19 cases. Critically, I3C, a natural NEDD4 and WWP1 inhibitor from Brassicaceae, displays potent antiviral effects and inhibits viral egression. In conclusion, we identify the HECT family members of E3 ligases as likely novel biomarkers for COVID-19, as well as new potential targets of therapeutic strategy easily testable in clinical trials in view of the established well-tolerated nature of the Brassicaceae natural compounds.

Subjects

Subjects :
Cytology
QH573-671

Details

Language :
English
ISSN :
20414889
Volume :
12
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Cell Death and Disease
Publication Type :
Academic Journal
Accession number :
edsdoj.44bb55f6f8b74b5bb5433d1a15eac416
Document Type :
article
Full Text :
https://doi.org/10.1038/s41419-021-03513-1