Inhibition of HECT E3 ligases as potential therapy for COVID-19.
Adult
Aged
Animals
Antiviral Agents
/ pharmacology
COVID-19
/ enzymology
Chlorocebus aethiops
Endosomal Sorting Complexes Required for Transport
/ metabolism
Female
Humans
Indoles
/ pharmacology
Male
Mice
Mice, Inbred BALB C
Middle Aged
Nedd4 Ubiquitin Protein Ligases
/ genetics
SARS-CoV-2
/ isolation & purification
Spike Glycoprotein, Coronavirus
/ metabolism
Ubiquitin-Protein Ligases
/ antagonists & inhibitors
Ubiquitination
Vero Cells
COVID-19 Drug Treatment
Journal
Cell death & disease
ISSN: 2041-4889
Titre abrégé: Cell Death Dis
Pays: England
ID NLM: 101524092
Informations de publication
Date de publication:
24 03 2021
24 03 2021
Historique:
received:
28
01
2021
accepted:
05
02
2021
revised:
04
02
2021
entrez:
25
3
2021
pubmed:
26
3
2021
medline:
7
4
2021
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 33762578
doi: 10.1038/s41419-021-03513-1
pii: 10.1038/s41419-021-03513-1
pmc: PMC7987752
doi:
Substances chimiques
Antiviral Agents
0
Endosomal Sorting Complexes Required for Transport
0
Indoles
0
Spike Glycoprotein, Coronavirus
0
spike protein, SARS-CoV-2
0
indole-3-carbinol
C11E72455F
Nedd4 Ubiquitin Protein Ligases
EC 2.3.2.26
WWP1 protein, human
EC 2.3.2.26
Ubiquitin-Protein Ligases
EC 2.3.2.27
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
310Subventions
Organisme : Agence Nationale de la Recherche (French National Research Agency)
ID : ANR-10-LABX-62-IBEID
Organisme : Howard Hughes Medical Institute
Pays : United States
Organisme : NHGRI NIH HHS
ID : UM1 HG006504
Pays : United States
Organisme : NHGRI NIH HHS
ID : U24 HG008956
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI088364
Pays : United States
Organisme : Agence Nationale de la Recherche (French National Research Agency)
ID : ANR-10-IAHU-01
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