7E3K
Ultrapotent SARS-CoV-2 neutralizing antibodies with protective efficacy against newly emerged mutational variants
Summary for 7E3K
Entry DOI | 10.2210/pdb7e3k/pdb |
EMDB information | 30982 30983 |
Descriptor | Spike glycoprotein, 13G9 heavy chain, 13G9 light chain, ... (4 entities in total) |
Functional Keywords | covid-19, spike glycoprotein, virus, viral protein, antibody |
Biological source | Severe acute respiratory syndrome coronavirus 2 (2019-nCoV) More |
Total number of polymer chains | 9 |
Total formula weight | 573276.21 |
Authors | |
Primary citation | Li, T.,Han, X.,Gu, C.,Guo, H.,Zhang, H.,Wang, Y.,Hu, C.,Wang, K.,Liu, F.,Luo, F.,Zhang, Y.,Hu, J.,Wang, W.,Li, S.,Hao, Y.,Shen, M.,Huang, J.,Long, Y.,Song, S.,Wu, R.,Mu, S.,Chen, Q.,Gao, F.,Wang, J.,Long, S.,Li, L.,Wu, Y.,Gao, Y.,Xu, W.,Cai, X.,Qu, D.,Zhang, Z.,Zhang, H.,Li, N.,Gao, Q.,Zhang, G.,He, C.,Wang, W.,Ji, X.,Tang, N.,Yuan, Z.,Xie, Y.,Yang, H.,Zhang, B.,Huang, A.,Jin, A. Potent SARS-CoV-2 neutralizing antibodies with protective efficacy against newly emerged mutational variants. Nat Commun, 12:6304-6304, 2021 Cited by PubMed Abstract: Accumulating mutations in the SARS-CoV-2 Spike (S) protein can increase the possibility of immune escape, challenging the present COVID-19 prophylaxis and clinical interventions. Here, 3 receptor binding domain (RBD) specific monoclonal antibodies (mAbs), 58G6, 510A5 and 13G9, with high neutralizing potency blocking authentic SARS-CoV-2 virus display remarkable efficacy against authentic B.1.351 virus. Surprisingly, structural analysis has revealed that 58G6 and 13G9 both recognize the steric region S on the RBD, overlapping the E484K mutation presented in B.1.351. Also, 58G6 directly binds to another region S in the RBD. Significantly, 58G6 and 510A5 both demonstrate prophylactic efficacy against authentic SARS-CoV-2 and B.1.351 viruses in the transgenic mice expressing human ACE2 (hACE2), protecting weight loss and reducing virus loads. Together, we have evidenced 2 potent neutralizing Abs with unique mechanism targeting authentic SARS-CoV-2 mutants, which can be promising candidates to fulfill the urgent needs for the prolonged COVID-19 pandemic. PubMed: 34728625DOI: 10.1038/s41467-021-26539-7 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (3.9 Å) |
Structure validation
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