Summary for 8TM1
| Entry DOI | 10.2210/pdb8tm1/pdb |
| EMDB information | 41374 |
| Descriptor | Spike glycoprotein, N3-1 Fab heavy chain, N3-1 Fab light chain (3 entities in total) |
| Functional Keywords | sars-cov-2 spike, neutralizing antibody, rbd-directed antibody, quaternary epitope, viral protein, viral protein-immune system complex, viral protein/immune system |
| Biological source | Severe acute respiratory syndrome coronavirus 2 More |
| Total number of polymer chains | 4 |
| Total formula weight | 311138.92 |
| Authors | Hsieh, C.-L.,McLellan, J.S. (deposition date: 2023-07-27, release date: 2024-01-17, Last modification date: 2025-05-28) |
| Primary citation | Goike, J.,Hsieh, C.L.,Horton, A.P.,Gardner, E.C.,Zhou, L.,Bartzoka, F.,Wang, N.,Javanmardi, K.,Herbert, A.,Abbassi, S.,Xie, X.,Xia, H.,Shi, P.Y.,Renberg, R.,Segall-Shapiro, T.H.,Terrace, C.I.,Wu, W.,Shroff, R.,Byrom, M.,Ellington, A.D.,Marcotte, E.M.,Musser, J.M.,Kuchipudi, S.V.,Kapur, V.,Georgiou, G.,Weaver, S.C.,Dye, J.M.,Boutz, D.R.,McLellan, J.S.,Gollihar, J.D. SARS-COV-2 Omicron variants conformationally escape a rare quaternary antibody binding mode. Commun Biol, 6:1250-1250, 2023 Cited by PubMed Abstract: The ongoing evolution of SARS-CoV-2 into more easily transmissible and infectious variants has provided unprecedented insight into mutations enabling immune escape. Understanding how these mutations affect the dynamics of antibody-antigen interactions is crucial to the development of broadly protective antibodies and vaccines. Here we report the characterization of a potent neutralizing antibody (N3-1) identified from a COVID-19 patient during the first disease wave. Cryogenic electron microscopy revealed a quaternary binding mode that enables direct interactions with all three receptor-binding domains of the spike protein trimer, resulting in extraordinary avidity and potent neutralization of all major variants of concern until the emergence of Omicron. Structure-based rational design of N3-1 mutants improved binding to all Omicron variants but only partially restored neutralization of the conformationally distinct Omicron BA.1. This study provides new insights into immune evasion through changes in spike protein dynamics and highlights considerations for future conformationally biased multivalent vaccine designs. PubMed: 38082099DOI: 10.1038/s42003-023-05649-6 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (2.79 Å) |
Structure validation
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