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7Q1Z

Structure of formaldehyde cross-linked SARS-CoV-2 S glycoprotein

Summary for 7Q1Z
Entry DOI10.2210/pdb7q1z/pdb
EMDB information13776
DescriptorSpike glycoprotein, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose (3 entities in total)
Functional Keywordssars-cov-2, glycoprotein, immunization, viral protein
Biological sourceSevere acute respiratory syndrome coronavirus 2 (2019-nCoV, SARS-CoV-2)
Total number of polymer chains3
Total formula weight440864.00
Authors
Sulbaran, G.,Effantin, G.,Schoehn, G.,Weissenhorn, W. (deposition date: 2021-10-22, release date: 2022-03-09, Last modification date: 2024-11-20)
Primary citationSulbaran, G.,Maisonnasse, P.,Amen, A.,Effantin, G.,Guilligay, D.,Dereuddre-Bosquet, N.,Burger, J.A.,Poniman, M.,Grobben, M.,Buisson, M.,Dergan Dylon, S.,Naninck, T.,Lemaitre, J.,Gros, W.,Gallouet, A.S.,Marlin, R.,Bouillier, C.,Contreras, V.,Relouzat, F.,Fenel, D.,Thepaut, M.,Bally, I.,Thielens, N.,Fieschi, F.,Schoehn, G.,van der Werf, S.,van Gils, M.J.,Sanders, R.W.,Poignard, P.,Le Grand, R.,Weissenhorn, W.
Immunization with synthetic SARS-CoV-2 S glycoprotein virus-like particles protects macaques from infection.
Cell Rep Med, 3:100528-100528, 2022
Cited by
PubMed Abstract: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has caused an ongoing global health crisis. Here, we present as a vaccine candidate synthetic SARS-CoV-2 spike (S) glycoprotein-coated lipid vesicles that resemble virus-like particles. Soluble S glycoprotein trimer stabilization by formaldehyde cross-linking introduces two major inter-protomer cross-links that keep all receptor-binding domains in the "down" conformation. Immunization of cynomolgus macaques with S coated onto lipid vesicles (S-LVs) induces high antibody titers with potent neutralizing activity against the vaccine strain, Alpha, Beta, and Gamma variants as well as T helper (Th)1 CD4-biased T cell responses. Although anti-receptor-binding domain (RBD)-specific antibody responses are initially predominant, the third immunization boosts significant non-RBD antibody titers. Challenging vaccinated animals with SARS-CoV-2 shows a complete protection through sterilizing immunity, which correlates with the presence of nasopharyngeal anti-S immunoglobulin G (IgG) and IgA titers. Thus, the S-LV approach is an efficient and safe vaccine candidate based on a proven classical approach for further development and clinical testing.
PubMed: 35233549
DOI: 10.1016/j.xcrm.2022.100528
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.4 Å)
Structure validation

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