5FV1
Crystal structure of hVEGF in complex with VK domain antibody
5FV1 の概要
エントリーDOI | 10.2210/pdb5fv1/pdb |
関連するPDBエントリー | 5FV2 |
分子名称 | VK DOMAIN ANTIBODY, VASCULAR ENDOTHELIAL GROWTH FACTOR A (3 entities in total) |
機能のキーワード | immune system, vegf, domain antibody, vascular endothelial growth factor |
由来する生物種 | HOMO SAPIENS (HUMAN) 詳細 |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 51183.96 |
構造登録者 | |
主引用文献 | Walker, A.,Chung, C.,Neu, M.,Burman, M.,Batuwangala, T.,Jones, G.,Tang, C.,Steward, M.,Mullin, M.,Tournier, N.,Lewis, A.,Korczynska, J.,Chung, V.,Catchpole, I. Novel Interaction Mechanism of a Domain Antibody Based Inhibitor of Human Vascular Endothelial Growth Factor with Greater Potency Than Ranibizumab and Bevacizumab and Improved Capacity Over Aflibercept. J.Biol.Chem., 291:5500-, 2016 Cited by PubMed Abstract: A potent VEGF inhibitor with novel antibody architecture and antigen binding mode has been developed. The molecule, hereafter referred to as VEGF dual dAb (domain antibody), was evaluated in vitro for binding to VEGF and for potency in VEGF-driven models and compared with other anti-VEGF biologics that have been used in ocular anti-angiogenic therapeutic regimes. VEGF dual dAb is more potent than bevacizumab and ranibizumab for VEGF binding, inhibition of VEGF receptor binding assays (RBAs), and VEGF-driven in vitro models of angiogenesis and displays comparable inhibition to aflibercept (Eylea). VEGF dual dAb is dimeric, and each monomer contains two distinct anti-VEGF domain antibodies attached via linkers to a human IgG1 Fc domain. Mechanistically, the enhanced in vitro potency of VEGF dual dAb, in comparison to other anti-VEGF biologics, can be explained by increased binding stoichiometry. A consistent model of the target engagement has been built based on the x-ray complexes of each of the two isolated domain antibodies with the VEGF antigen. PubMed: 26728464DOI: 10.1074/JBC.M115.691162 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.7 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード
