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8G77

SARS-CoV-2 spike/Nb6 complex

Summary for 8G77
Entry DOI10.2210/pdb8g77/pdb
EMDB information29792 29793 29794 29795 29796 29797 29798 29799 29802 29803 29804 29805 29806
DescriptorSpike glycoprotein, Nanosota-6, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
Functional Keywordssars-cov-2, viral protein-immune system complex, nanobody, viral protein/immune system
Biological sourceSevere acute respiratory syndrome coronavirus 2
More
Total number of polymer chains6
Total formula weight469821.69
Authors
Ye, G.,Bu, F.,Liu, B.,Li, F. (deposition date: 2023-02-16, release date: 2024-02-21, Last modification date: 2024-10-30)
Primary citationYe, G.,Bu, F.,Pan, R.,Mendoza, A.,Saxena, D.,Zheng, J.,Perlman, S.,Liu, B.,Li, F.
Dual-role epitope on SARS-CoV-2 spike enhances and neutralizes viral entry across different variants.
Plos Pathog., 20:e1012493-e1012493, 2024
Cited by
PubMed Abstract: Grasping the roles of epitopes in viral glycoproteins is essential for unraveling the structure and function of these proteins. Up to now, all identified epitopes have been found to either neutralize, have no effect on, or enhance viral entry into cells. Here, we used nanobodies (single-domain antibodies) as probes to investigate a unique epitope on the SARS-CoV-2 spike protein, located outside the protein's receptor-binding domain. Nanobody binding to this epitope enhances the cell entry of prototypic SARS-CoV-2, while neutralizing the cell entry of SARS-CoV-2 Omicron variant. Moreover, nanobody binding to this epitope promotes both receptor binding activity and post-attachment activity of prototypic spike, explaining the enhanced viral entry. The opposite occurs with Omicron spike, explaining the neutralized viral entry. This study reveals a unique epitope that can both enhance and neutralize viral entry across distinct viral variants, suggesting that epitopes may vary their roles depending on the viral context. Consequently, antibody therapies should be assessed across different viral variants to confirm their efficacy and safety.
PubMed: 39236072
DOI: 10.1371/journal.ppat.1012493
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.8 Å)
Structure validation

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