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6JFI

The symmetric-reconstructed cryo-EM structure of Zika virus-FabZK2B10 complex

Summary for 6JFI
Entry DOI10.2210/pdb6jfi/pdb
Related6JEP
EMDB information9811 9812
DescriptorZIKV structural protein E, strutural protein M, FabZK2B10 heavy chain, ... (4 entities in total)
Functional Keywordszikv, antibody, virus
Biological sourceZika virus
More
Total number of polymer chains10
Total formula weight284381.62
Authors
Wang, L.,Wang, R.K.,Wang, L.,Ben, H.J.,Yu, L.,Gao, F.,Shi, X.L.,Yin, C.B.,Zhang, F.C.,Xiang, Y.,Zhang, L.Q. (deposition date: 2019-02-08, release date: 2019-04-10, Last modification date: 2024-03-27)
Primary citationWang, L.,Wang, R.,Wang, L.,Ben, H.,Yu, L.,Gao, F.,Shi, X.,Yin, C.,Zhang, F.,Xiang, Y.,Zhang, L.
Structural Basis for Neutralization and Protection by a Zika Virus-Specific Human Antibody.
Cell Rep, 26:3360-3368.e5, 2019
Cited by
PubMed Abstract: We previously reported a human monoclonal antibody, ZK2B10, capable of protection against Zika virus (ZIKV) infection and microcephaly in developing mouse embryos. Here, we report the structural features and mechanism of action of ZK2B10. The crystal structure at a resolution of 2.32 Å revealed that the epitope is located on the lateral ridge of DIII of the envelope glycoprotein. Cryo-EM structure with mature ZIKV showed that the antibody binds to DIIIs around the icosahedral 2-fold, 3-fold, and 5-fold axes, a distinct feature compared to those reported for DIII-specific antibodies. The binding of ZK2B10 to ZIKV has no detectable effect on viral attachment to target cells or on conformational changes of the E glycoprotein in the acidic environment, suggesting that ZK2B10 functions at steps between the formation of the fusion intermediate and membrane fusion. These results provide structural and mechanistic insights into how ZK2B10 mediates protection against ZIKV infection.
PubMed: 30893607
DOI: 10.1016/j.celrep.2019.02.062
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (11 Å)
Structure validation

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