7CAI
SARS-CoV-2 S trimer with two RBDs in the open state and complexed with two H014 Fab
Summary for 7CAI
Entry DOI | 10.2210/pdb7cai/pdb |
EMDB information | 30332 |
Descriptor | Spike glycoprotein, Light chain of H014 Fab, Heavy chain of H014 Fab, ... (5 entities in total) |
Functional Keywords | sars-cov-2 spike glycoprotein, neutralizing antibody, viral protein |
Biological source | Severe acute respiratory syndrome coronavirus 2 (2019-nCoV) More |
Total number of polymer chains | 7 |
Total formula weight | 508823.55 |
Authors | |
Primary citation | Lv, Z.,Deng, Y.Q.,Ye, Q.,Cao, L.,Sun, C.Y.,Fan, C.,Huang, W.,Sun, S.,Sun, Y.,Zhu, L.,Chen, Q.,Wang, N.,Nie, J.,Cui, Z.,Zhu, D.,Shaw, N.,Li, X.F.,Li, Q.,Xie, L.,Wang, Y.,Rao, Z.,Qin, C.F.,Wang, X. Structural basis for neutralization of SARS-CoV-2 and SARS-CoV by a potent therapeutic antibody. Science, 369:1505-1509, 2020 Cited by PubMed Abstract: The coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in an unprecedented public health crisis. There are no approved vaccines or therapeutics for treating COVID-19. Here we report a humanized monoclonal antibody, H014, that efficiently neutralizes SARS-CoV-2 and SARS-CoV pseudoviruses as well as authentic SARS-CoV-2 at nanomolar concentrations by engaging the spike (S) receptor binding domain (RBD). H014 administration reduced SARS-CoV-2 titers in infected lungs and prevented pulmonary pathology in a human angiotensin-converting enzyme 2 mouse model. Cryo-electron microscopy characterization of the SARS-CoV-2 S trimer in complex with the H014 Fab fragment unveiled a previously uncharacterized conformational epitope, which was only accessible when the RBD was in an open conformation. Biochemical, cellular, virological, and structural studies demonstrated that H014 prevents attachment of SARS-CoV-2 to its host cell receptors. Epitope analysis of available neutralizing antibodies against SARS-CoV and SARS-CoV-2 uncovered broad cross-protective epitopes. Our results highlight a key role for antibody-based therapeutic interventions in the treatment of COVID-19. PubMed: 32703908DOI: 10.1126/science.abc5881 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (3.49 Å) |
Structure validation
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