Cytoplasmic Tail Truncation Stabilizes S1-S2 Association and Enhances S Protein Incorporation into SARS-CoV-2 Pseudovirions
Author:
Affiliation:
1. Department of Immunology and Microbiology, Scripps Biomedical Research at the University of Florida, Jupiter, Florida, USA
2. Department of Medicinal Chemistry, University of Washington, Seattle, Washington, USA
Abstract
Funder
HHS | NIH | National Institute of Allergy and Infectious Diseases
HHS | National Institutes of Health
HHS | NIH | National Institute of General Medical Sciences
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Link
https://journals.asm.org/doi/pdf/10.1128/jvi.01650-22
Reference48 articles.
1. A structural analysis of M protein in coronavirus assembly and morphology
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4. Cathepsin L Functionally Cleaves the Severe Acute Respiratory Syndrome Coronavirus Class I Fusion Protein Upstream of Rather than Adjacent to the Fusion Peptide
5. SARS Coronavirus, but Not Human Coronavirus NL63, Utilizes Cathepsin L to Infect ACE2-expressing Cells
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