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9ATZ

HIV 16055.v8.3 SOSIP Env in Complex with V2 Epitope and Anti-Immune Complex pAbs from Rabbit 2464

This is a non-PDB format compatible entry.
Summary for 9ATZ
Entry DOI10.2210/pdb9atz/pdb
EMDB information43838
DescriptorRabbit V2 Polyclonal Antibody - Predicted Light Chain, Rabbit Anti-Immune Complex Antibody - Predicted Light Chain, Rabbit V2 Polyclonal Antibody - Predicted Heavy Chain, ... (9 entities in total)
Functional Keywordshiv, polyclonal, antibodies, cryoempem, rabbit, anti-immune complex, v1/v3, viral protein
Biological sourceHuman immunodeficiency virus 1
More
Total number of polymer chains18
Total formula weight358489.68
Authors
Brown, S.,Antansijevic, A.,Ward, A.B. (deposition date: 2024-02-27, release date: 2025-01-29)
Primary citationBrown, S.,Antanasijevic, A.,Sewall, L.M.,Garcia, D.M.,Brouwer, P.J.M.,Sanders, R.W.,Ward, A.B.
Anti-immune complex antibodies are elicited during repeated immunization with HIV Env immunogens.
Sci Immunol, 10:eadp5218-eadp5218, 2025
Cited by
PubMed Abstract: Vaccination strategies against HIV-1 aim to elicit broadly neutralizing antibodies (bnAbs) using prime-boost regimens with HIV envelope (Env) immunogens. Epitope mapping has shown that early antibody responses are directed to easily accessible nonneutralizing epitopes on Env instead of bnAb epitopes. Autologously neutralizing antibody responses appear upon boosting, once immunodominant epitopes are saturated. Here, we use electron microscopy-based polyclonal epitope mapping (EMPEM) to elucidate how repeated immunization with HIV Env SOSIP immunogens results in the generation of Ab2α anti-idiotypic antibodies in rabbits and rhesus macaques. We present the structures of six anti-immune complex antibodies and find that they target idiotopes composed of framework regions of antibodies bound to Env. Examination of cryo-electron microscopy density enabled prediction of sequences for an anti-immune complex antibody, the paratope of which is enriched with aromatic amino acids. This work sheds light on current vaccine development efforts for HIV, as well as for other pathogens in which repeated exposure to antigen is required.
PubMed: 39823319
DOI: 10.1126/sciimmunol.adp5218
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.4 Å)
Structure validation

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