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8C8T

cryo-EM structure of BG505 SOSIP.664 HIV-1 Env trimer in complex with bNAbs EPTC112 and 3BNC117

This is a non-PDB format compatible entry.
Summary for 8C8T
Entry DOI10.2210/pdb8c8t/pdb
EMDB information16493
DescriptorEnvelope glycoprotein gp160, 2-acetamido-2-deoxy-beta-D-glucopyranose, Gp41 Bg505 T332n Sosip.664, ... (10 entities in total)
Functional Keywordshiv, post-treatment controller, broadly neutralizing antibodies, v3-site, immune system
Biological sourceHuman immunodeficiency virus 1
More
Total number of polymer chains14
Total formula weight410177.48
Authors
Baquero, E.,Molinos-Albert, L.,Mouquet, H. (deposition date: 2023-01-21, release date: 2023-07-05, Last modification date: 2024-11-06)
Primary citationMolinos-Albert, L.M.,Baquero, E.,Bouvin-Pley, M.,Lorin, V.,Charre, C.,Planchais, C.,Dimitrov, J.D.,Monceaux, V.,Vos, M.,Hocqueloux, L.,Berger, J.L.,Seaman, M.S.,Braibant, M.,Avettand-Fenoel, V.,Saez-Cirion, A.,Mouquet, H.
Anti-V1/V3-glycan broadly HIV-1 neutralizing antibodies in a post-treatment controller.
Cell Host Microbe, 31:1275-, 2023
Cited by
PubMed Abstract: HIV-1 broadly neutralizing antibodies (bNAbs) can decrease viremia but are usually unable to counteract autologous viruses escaping the antibody pressure. Nonetheless, bNAbs may contribute to natural HIV-1 control in individuals off antiretroviral therapy (ART). Here, we describe a bNAb B cell lineage elicited in a post-treatment controller (PTC) that exhibits broad seroneutralization and show that a representative antibody from this lineage, EPTC112, targets a quaternary epitope in the glycan-V3 loop supersite of the HIV-1 envelope glycoprotein. The cryo-EM structure of EPTC112 complexed with soluble BG505 SOSIP.664 envelope trimers revealed interactions with N301- and N156-branched N-glycans and the GDIR V3 loop motif. Although the sole contemporaneous virus circulating in this PTC was resistant to EPTC112, it was potently neutralized by autologous plasma IgG antibodies. Our findings illuminate how cross-neutralizing antibodies can alter the HIV-1 infection course in PTCs and may control viremia off-ART, supporting their role in functional HIV-1 cure strategies.
PubMed: 37433296
DOI: 10.1016/j.chom.2023.06.006
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.2 Å)
Structure validation

238268

数据于2025-07-02公开中

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