Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.celrep.2020.107584
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dc.titleA Human Antibody Neutralizes Different Flaviviruses by Using Different Mechanisms
dc.contributor.authorZhang, S.
dc.contributor.authorLoy, T.
dc.contributor.authorNg, T.-S.
dc.contributor.authorLim, X.-N.
dc.contributor.authorChew, S.-Y.V.
dc.contributor.authorTan, T.Y.
dc.contributor.authorXu, M.
dc.contributor.authorKostyuchenko, V.A.
dc.contributor.authorTukijan, F.
dc.contributor.authorShi, J.
dc.contributor.authorFink, K.
dc.contributor.authorLok, S.-M.
dc.date.accessioned2021-08-24T02:35:00Z
dc.date.available2021-08-24T02:35:00Z
dc.date.issued2020
dc.identifier.citationZhang, S., Loy, T., Ng, T.-S., Lim, X.-N., Chew, S.-Y.V., Tan, T.Y., Xu, M., Kostyuchenko, V.A., Tukijan, F., Shi, J., Fink, K., Lok, S.-M. (2020). A Human Antibody Neutralizes Different Flaviviruses by Using Different Mechanisms. Cell Reports 31 (4) : 107584. ScholarBank@NUS Repository. https://doi.org/10.1016/j.celrep.2020.107584
dc.identifier.issn2211-1247
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/198914
dc.description.abstractHuman antibody SIgN-3C neutralizes dengue virus (DENV) and Zika virus (ZIKV) differently. DENV:SIgN-3C Fab and ZIKV:SIgN-3C Fab cryoelectron microscopy (cryo-EM) complex structures show Fabs crosslink E protein dimers at extracellular pH 8.0 condition and also when further incubated at acidic endosomal conditions (pH 8.0–6.5). We observe Fab binding to DENV (pH 8.0–5.0) prevents virus fusion, and the number of bound Fabs increase (from 120 to 180). For ZIKV, although there are already 180 copies of Fab at pH 8.0, virus structural changes at pH 5.0 are not inhibited. The immunoglobulin G (IgG):DENV structure at pH 8.0 shows both Fab arms bind to epitopes around the 2-fold vertex. On ZIKV, an additional Fab around the 5-fold vertex at pH 8.0 suggests one IgG arm would engage with an epitope, although the other may bind to other viruses, causing aggregation. For DENV2 at pH 5.0, a similar scenario would occur, suggesting DENV2:IgG complex would aggregate in the endosome. Hence, a single antibody employs different neutralization mechanisms against different flaviviruses. Zhang et al. show that a human monoclonal antibody SIgN-3C can neutralize closely related dengue and Zika virus via different mechanisms. The antibody neutralizes dengue virus by preventing virus:endosomal membrane fusion, although it aggregates Zika virus particles extracellularly. © 2020 The Author(s)
dc.publisherElsevier B.V.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScopus OA2020
dc.subjectcryoEM structure
dc.subjectdengue virus
dc.subjecthuman antibody
dc.subjectmembrane fusion
dc.subjectvirus aggregation
dc.subjectvirus neutralization
dc.subjectzika virus
dc.typeArticle
dc.contributor.departmentDEPT OF BIOLOGICAL SCIENCES
dc.contributor.departmentDEPT OF MICROBIOLOGY & IMMUNOLOGY
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1016/j.celrep.2020.107584
dc.description.sourcetitleCell Reports
dc.description.volume31
dc.description.issue4
dc.description.page107584
dc.published.statePublished
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