7E3B
SARS-Cov-2 spike in complex with the Ab5 neutralizing antibody (focused refinement on Fab-RBD)
Summary for 7E3B
Entry DOI | 10.2210/pdb7e3b/pdb |
EMDB information | 30978 |
Descriptor | Spike protein S1, Heavy Chain of Ab5, Light Chain of Ab5, ... (4 entities in total) |
Functional Keywords | spike, sars-cov-2, antibody, viral protein, viral protein-immune system complex, viral protein/immune system |
Biological source | Severe acute respiratory syndrome coronavirus 2 (2019-nCoV) More |
Total number of polymer chains | 3 |
Total formula weight | 94928.94 |
Authors | |
Primary citation | Nie, J.,Xie, J.,Liu, S.,Wu, J.,Liu, C.,Li, J.,Liu, Y.,Wang, M.,Zhao, H.,Zhang, Y.,Yao, J.,Chen, L.,Shen, Y.,Yang, Y.,Wang, H.W.,Wang, Y.,Huang, W. Three epitope-distinct human antibodies from RenMab mice neutralize SARS-CoV-2 and cooperatively minimize the escape of mutants. Cell Discov, 7:53-53, 2021 Cited by PubMed Abstract: Coronavirus disease 2019 (COVID-19), a pandemic disease caused by the newly emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has caused more than 3.8 million deaths to date. Neutralizing antibodies are effective therapeutic measures. However, many naturally occurring mutations at the receptor-binding domain (RBD) have emerged, and some of them can evade existing neutralizing antibodies. Here, we utilized RenMab, a novel mouse carrying the entire human antibody variable region, for neutralizing antibody discovery. We obtained several potent RBD-blocking antibodies and categorized them into four distinct groups by epitope mapping. We determined the involved residues of the epitope of three representative antibodies by cryo-electron microscopy (Cryo-EM) studies. Moreover, we performed neutralizing experiments with 50 variant strains with single or combined mutations and found that the mixing of three epitope-distinct antibodies almost eliminated the mutant escape. Our study provides a sound basis for the rational design of fully human antibody cocktails against SARS-CoV-2 and pre-emergent coronaviral threats. PubMed: 34285195DOI: 10.1038/s41421-021-00292-z PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (4.2 Å) |
Structure validation
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