Structure-guided covalent stabilization of coronavirus spike glycoprotein trimers in the closed conformation

• Published in: Nature structural & molecular biology Vol. 27; no. 10; pp. 942 - 949
• Main Authors: McCallum, Matthew, Walls, Alexandra C., Bowen, John E., Corti, Davide, Veesler, David
• Format: Journal Article
• Language: English
• Published: New York Nature Publishing Group US 01.10.2020; Nature Publishing Group
• Subjects: 101/28; 631/326/596/4130; 631/535/1258/1259; Antibodies, Monoclonal - metabolism; Antibodies, Neutralizing - metabolism; Betacoronavirus - chemistry; Betacoronavirus - genetics; Betacoronavirus - immunology; Betacoronavirus - metabolism; Biochemistry; Biological Microscopy; Biomedical and Life Sciences; Causes of; Conformation; Coronaviruses; Cryoelectron Microscopy; Disulfides - chemistry; Electrophoresis, Polyacrylamide Gel; Enzyme-Linked Immunosorbent Assay; Epidemics; Genetic aspects; Glycoproteins; Health aspects; Humans; Life Sciences; Membrane Biology; Models, Molecular; Mutation; Properties; Protein Conformation; Protein Domains; Protein Engineering; Protein Multimerization; Protein Stability; Protein Structure; Proteins; SARS-CoV-2; Spike Glycoprotein, Coronavirus - chemistry; Spike Glycoprotein, Coronavirus - genetics; Spike Glycoprotein, Coronavirus - immunology; Spike Glycoprotein, Coronavirus - metabolism; United States; Virulence (Microbiology); United States
• ISSN: 1545-9993; 1545-9985; 1545-9985
• DOI: 10.1038/s41594-020-0483-8

SARS-CoV-2 is the causative agent of the COVID-19 pandemic, with 10 million infections and more than 500,000 fatalities by June 2020. To initiate infection, the SARS-CoV-2 spike (S) glycoprotein promotes attachment to the host cell surface and fusion of the viral and host membranes. Prefusion SARS-CoV-2 S is the main target of neutralizing antibodies and the focus of vaccine design. However, its limited stability and conformational dynamics are limiting factors for developing countermeasures against this virus. We report here the design of a construct corresponding to the prefusion SARS-CoV-2 S ectodomain trimer, covalently stabilized by a disulfide bond in the closed conformation. Structural and antigenicity analyses show we successfully shut S in the closed state without otherwise altering its architecture. We demonstrate that this strategy is applicable to other β-coronaviruses, such as SARS-CoV and MERS-CoV, and might become an important tool for structural biology, serology, vaccine design and immunology studies. The conformational dynamics of SARS-CoV-2 spike are constrained by engineering a disulfide bond that locks the protein in a closed conformation, a strategy that was also applied to SARS-CoV and MERS-CoV.