7RYU
Anti-HIV neutralizing antibody Ab1303 Fab isolated from sequentially immunized mcaques
7RYU の概要
| エントリーDOI | 10.2210/pdb7ryu/pdb |
| 分子名称 | Ab1303 Fab heavy chain, Ab1303 Fab light chain (3 entities in total) |
| 機能のキーワード | anti-hiv neutralizing antibody; antibody fab;, immune system |
| 由来する生物種 | Macaca mulatta (Rhesus monkey) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 48758.15 |
| 構造登録者 | |
| 主引用文献 | Yang, Z.,Dam, K.A.,Bridges, M.D.,Hoffmann, M.A.G.,DeLaitsch, A.T.,Gristick, H.B.,Escolano, A.,Gautam, R.,Martin, M.A.,Nussenzweig, M.C.,Hubbell, W.L.,Bjorkman, P.J. Neutralizing antibodies induced in immunized macaques recognize the CD4-binding site on an occluded-open HIV-1 envelope trimer. Nat Commun, 13:732-732, 2022 Cited by PubMed Abstract: Broadly-neutralizing antibodies (bNAbs) against HIV-1 Env can protect from infection. We characterize Ab1303 and Ab1573, heterologously-neutralizing CD4-binding site (CD4bs) antibodies, isolated from sequentially-immunized macaques. Ab1303/Ab1573 binding is observed only when Env trimers are not constrained in the closed, prefusion conformation. Fab-Env cryo-EM structures show that both antibodies recognize the CD4bs on Env trimer with an 'occluded-open' conformation between closed, as targeted by bNAbs, and fully-open, as recognized by CD4. The occluded-open Env trimer conformation includes outwardly-rotated gp120 subunits, but unlike CD4-bound Envs, does not exhibit V1V2 displacement, 4-stranded gp120 bridging sheet, or co-receptor binding site exposure. Inter-protomer distances within trimers measured by double electron-electron resonance spectroscopy suggest an equilibrium between occluded-open and closed Env conformations, consistent with Ab1303/Ab1573 binding stabilizing an existing conformation. Studies of Ab1303/Ab1573 demonstrate that CD4bs neutralizing antibodies that bind open Env trimers can be raised by immunization, thereby informing immunogen design and antibody therapeutic efforts. PubMed: 35136084DOI: 10.1038/s41467-022-28424-3 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.51 Å) |
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