9AXD

HIV BG505.v5.2 (N289/N241) SOSIP Env in Complex with gp120-Interface pAb from Rh.33203

これはPDB形式変換不可エントリーです。

9AXD の概要

• エントリーDOI: 10.2210/pdb9axd/pdb
• EMDBエントリー: 43935
• 分子名称: gp120-Interface Polyclonal Antibody - Predicted Heavy Chain, gp120-Interface Polyclonal Antibody - Predicted Light Chain, Surface protein gp120, ... (8 entities in total)
• 機能のキーワード: hiv, polyclonal, antibodies, cryoempem, nhp, macaque, gp120-interface, viral protein
• 由来する生物種: Human immunodeficiency virus 1; 詳細
• タンパク質・核酸の鎖数: 8
• 化学式量合計: 266662.05

構造登録者

Brown, S.,Antansijevic, A.,Ward, A.B. (登録日: 2024-03-06, 公開日: 2025-01-29, 最終更新日: 2025-06-04)

主引用文献

Brown, 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

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

実験手法

ELECTRON MICROSCOPY (3.8 Å)