Spike substitutions E484D, P812R and Q954H mediate ACE2-independent entry of SARS-CoV-2 across different cell lines.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which causes coronavirus disease 2019 (COVID-19), has evolved into variants with multiple spike protein coding mutations that affect its transmissibility, infectivity, and immune evasion, in particular from neutralizing antibodies. Severa...
Saved in:
| Main Authors: | Greta Vizgirda, Alexander P Underwood, Ulrik Fahnøe, Nina Weis, Santseharay Ramirez, Jens Bukh |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2025-01-01
|
| Series: | PLoS ONE |
| Online Access: | https://doi.org/10.1371/journal.pone.0326419 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Neutralisation resistance of SARS-CoV-2 spike-variants is primarily mediated by synergistic receptor binding domain substitutions
by: Long V. Pham, et al.
Published: (2024-12-01) -
Critical amino acid residues in human ACE2 for SARS-CoV-2 spike protein binding and virus entry
by: Weiyi Chen, et al.
Published: (2025-08-01) -
Higher Rates of Viral Evolution in Chronic Hepatitis B Patients Linked to Predicted T Cell Epitopes
by: Magnus Illum Dalegaard, et al.
Published: (2025-05-01) -
HKU5 bat merbecoviruses engage bat and mink ACE2 as entry receptors
by: Mia Madel Alfajaro, et al.
Published: (2025-07-01) -
The Renin–Angiotensin System Modulates SARS-CoV-2 Entry via ACE2 Receptor
by: Sophia Gagliardi, et al.
Published: (2025-07-01)