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4ZFG

Dual-specificity Fab 5A12 in complex with Angiopoietin 2

4ZFG の概要
エントリーDOI10.2210/pdb4zfg/pdb
関連するPDBエントリー4ZFF
分子名称Angiopoietin-2, Fragment antigen binding 5A12 heavy chain, Fragment antigen binding 5A12 light chain, ... (6 entities in total)
機能のキーワードfab, daf, angiogenesis, tie receptor, signaling protein-immune system complex, signaling protein/immune system
由来する生物種Homo sapiens (Human)
詳細
細胞内の位置Secreted: O15123
タンパク質・核酸の鎖数3
化学式量合計74482.83
構造登録者
Harris, S.F.,Wu, P. (登録日: 2015-04-21, 公開日: 2015-07-01, 最終更新日: 2024-11-06)
主引用文献Koenig, P.,Lee, C.V.,Sanowar, S.,Wu, P.,Stinson, J.,Harris, S.F.,Fuh, G.
Deep Sequencing-guided Design of a High Affinity Dual Specificity Antibody to Target Two Angiogenic Factors in Neovascular Age-related Macular Degeneration.
J.Biol.Chem., 290:21773-21786, 2015
Cited by
PubMed Abstract: The development of dual targeting antibodies promises therapies with improved efficacy over mono-specific antibodies. Here, we engineered a Two-in-One VEGF/angiopoietin 2 antibody with dual action Fab (DAF) as a potential therapeutic for neovascular age-related macular degeneration. Crystal structures of the VEGF/angiopoietin 2 DAF in complex with its two antigens showed highly overlapping binding sites. To achieve sufficient affinity of the DAF to block both angiogenic factors, we turned to deep mutational scanning in the complementarity determining regions (CDRs). By mutating all three CDRs of each antibody chain simultaneously, we were able not only to identify affinity improving single mutations but also mutation pairs from different CDRs that synergistically improve both binding functions. Furthermore, insights into the cooperativity between mutations allowed us to identify fold-stabilizing mutations in the CDRs. The data obtained from deep mutational scanning reveal that the majority of the 52 CDR residues are utilized differently for the two antigen binding function and permit, for the first time, the engineering of several DAF variants with sub-nanomolar affinity against two structurally unrelated antigens. The improved variants show similar blocking activity of receptor binding as the high affinity mono-specific antibodies against these two proteins, demonstrating the feasibility of generating a dual specificity binding surface with comparable properties to individual high affinity mono-specific antibodies.
PubMed: 26088137
DOI: 10.1074/jbc.M115.662783
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.27 Å)
構造検証レポート
Validation report summary of 4zfg
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-07-09に公開中

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