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PDBsum entry 7cwl

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protein ligands Protein-protein interface(s) links
Viral protein PDB id
7cwl

 

 

 

 

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Contents
Protein chains
1073 a.a.
120 a.a.
108 a.a.
Ligands
NAG ×27
PDB id:
7cwl
Name: Viral protein
Title: Sars-cov-2 spike protein and p17 fab complex with one rbd in close state
Structure: Spike glycoprotein. Chain: a, b, c. Synonym: s glycoprotein,e2,peplomer protein. Engineered: yes. Fab p17 heavy chain. Chain: g, h, i. Engineered: yes. Fab p17 light chain. Chain: l, j, k.
Source: Severe acute respiratory syndrome coronavirus 2. 2019-ncov. Organism_taxid: 2697049. Gene: s, 2. Expressed in: homo sapiens. Expression_system_taxid: 9606. Expression_system_cell_line: hek293. Homo sapiens.
Authors: X.Wang,N.Wang
Key ref: H.Yao et al. (2021). Rational development of a human antibody cocktail that deploys multiple functions to confer Pan-SARS-CoVs protection. Cell Res, 31, 25-36. PubMed id: 33262452 DOI: 10.1107/S0907444909042073
Date:
29-Aug-20     Release date:   27-Jan-21    
PROCHECK
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 Headers
 References

Protein chains
P0DTC2  (SPIKE_SARS2) -  Spike glycoprotein from Severe acute respiratory syndrome coronavirus 2
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1273 a.a.
1073 a.a.
Protein chains
No UniProt id for this chain
Struc: 120 a.a.
Protein chains
No UniProt id for this chain
Struc: 108 a.a.
Key:    PfamA domain  Secondary structure

 

 
DOI no: 10.1107/S0907444909042073 Cell Res 31:25-36 (2021)
PubMed id: 33262452  
 
 
Rational development of a human antibody cocktail that deploys multiple functions to confer Pan-SARS-CoVs protection.
H.Yao, Y.Sun, Y.Q.Deng, N.Wang, Y.Tan, N.N.Zhang, X.F.Li, C.Kong, Y.P.Xu, Q.Chen, T.S.Cao, H.Zhao, X.Yan, L.Cao, Z.Lv, D.Zhu, R.Feng, N.Wu, W.Zhang, Y.Hu, K.Chen, R.R.Zhang, Q.Lv, S.Sun, Y.Zhou, R.Yan, G.Yang, X.Sun, C.Liu, X.Lu, L.Cheng, H.Qiu, X.Y.Huang, T.Weng, D.Shi, W.Jiang, J.Shao, L.Wang, J.Zhang, T.Jiang, G.Lang, C.F.Qin, L.Li, X.Wang.
 
  ABSTRACT  
 
Structural principles underlying the composition and synergistic mechanisms of protective monoclonal antibody cocktails are poorly defined. Here, we exploited antibody cooperativity to develop a therapeutic antibody cocktail against SARS-CoV-2. On the basis of our previously identified humanized cross-neutralizing antibody H014, we systematically analyzed a fully human naive antibody library and rationally identified a potent neutralizing antibody partner, P17, which confers effective protection in animal model. Cryo-EM studies dissected the nature of the P17 epitope, which is SARS-CoV-2 specific and distinctly different from that of H014. High-resolution structure of the SARS-CoV-2 spike in complex with H014 and P17, together with functional investigations revealed that in a two-antibody cocktail, synergistic neutralization was achieved by S1 shielding and conformational locking, thereby blocking receptor attachment and viral membrane fusion, conferring high potency as well as robustness against viral mutation escape. Furthermore, cluster analysis identified a hypothetical 3rd antibody partner for further reinforcing the cocktail as pan-SARS-CoVs therapeutics.
 

 

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