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7E8F

SARS-CoV-2 NTD in complex with N9 Fab

Summary for 7E8F
Entry DOI10.2210/pdb7e8f/pdb
EMDB information31017
DescriptorSpike protein S1, N9 H, N9 L, ... (8 entities in total)
Functional Keywordssars-cov-2, complex, antibody, viral protein
Biological sourceSevere acute respiratory syndrome coronavirus 2 (2019-nCoV, SARS-CoV-2)
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Total number of polymer chains8
Total formula weight199903.53
Authors
Du, S.,Xiao, J.,Zhang, Z. (deposition date: 2021-03-01, release date: 2021-06-09, Last modification date: 2024-10-16)
Primary citationCao, Y.,Yisimayi, A.,Bai, Y.,Huang, W.,Li, X.,Zhang, Z.,Yuan, T.,An, R.,Wang, J.,Xiao, T.,Du, S.,Ma, W.,Song, L.,Li, Y.,Li, X.,Song, W.,Wu, J.,Liu, S.,Li, X.,Zhang, Y.,Su, B.,Guo, X.,Wei, Y.,Gao, C.,Zhang, N.,Zhang, Y.,Dou, Y.,Xu, X.,Shi, R.,Lu, B.,Jin, R.,Ma, Y.,Qin, C.,Wang, Y.,Feng, Y.,Xiao, J.,Xie, X.S.
Humoral immune response to circulating SARS-CoV-2 variants elicited by inactivated and RBD-subunit vaccines.
Cell Res., 31:732-741, 2021
Cited by
PubMed Abstract: SARS-CoV-2 variants could induce immune escape by mutations on the receptor-binding domain (RBD) and N-terminal domain (NTD). Here we report the humoral immune response to circulating SARS-CoV-2 variants, such as 501Y.V2 (B.1.351), of the plasma and neutralizing antibodies (NAbs) elicited by CoronaVac (inactivated vaccine), ZF2001 (RBD-subunit vaccine) and natural infection. Among 86 potent NAbs identified by high-throughput single-cell VDJ sequencing of peripheral blood mononuclear cells from vaccinees and convalescents, near half anti-RBD NAbs showed major neutralization reductions against the K417N/E484K/N501Y mutation combination, with E484K being the dominant cause. VH3-53/VH3-66 recurrent antibodies respond differently to RBD variants, and K417N compromises the majority of neutralizing activity through reduced polar contacts with complementarity determining regions. In contrast, the 242-244 deletion (242-244Δ) would abolish most neutralization activity of anti-NTD NAbs by interrupting the conformation of NTD antigenic supersite, indicating a much less diversity of anti-NTD NAbs than anti-RBD NAbs. Plasma of convalescents and CoronaVac vaccinees displayed comparable neutralization reductions against pseudo- and authentic 501Y.V2 variants, mainly caused by E484K/N501Y and 242-244Δ, with the effects being additive. Importantly, RBD-subunit vaccinees exhibit markedly higher tolerance to 501Y.V2 than convalescents, since the elicited anti-RBD NAbs display a high diversity and are unaffected by NTD mutations. Moreover, an extended gap between the third and second doses of ZF2001 leads to better neutralizing activity and tolerance to 501Y.V2 than the standard three-dose administration. Together, these results suggest that the deployment of RBD-vaccines, through a third-dose boost, may be ideal for combating SARS-CoV-2 variants when necessary, especially for those carrying mutations that disrupt the NTD supersite.
PubMed: 34021265
DOI: 10.1038/s41422-021-00514-9
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.18 Å)
Structure validation

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