4I77
Lebrikizumab Fab bound to IL-13
4I77 の概要
| エントリーDOI | 10.2210/pdb4i77/pdb |
| 分子名称 | Lebrikizumab heavy chain, Lebrikizumab light chain, Interleukin-13, ... (4 entities in total) |
| 機能のキーワード | immunoglobulin, immune system recognition, immune system-cytokine complex, immune system/cytokine |
| 由来する生物種 | Homo sapiens 詳細 |
| 細胞内の位置 | Secreted: P35225 |
| タンパク質・核酸の鎖数 | 3 |
| 化学式量合計 | 59650.22 |
| 構造登録者 | |
| 主引用文献 | Ultsch, M.,Bevers, J.,Nakamura, G.,Vandlen, R.,Kelley, R.F.,Wu, L.C.,Eigenbrot, C. Structural Basis of Signaling Blockade by Anti-IL-13 Antibody Lebrikizumab. J.Mol.Biol., 425:1330-1339, 2013 Cited by PubMed Abstract: The cytokine interleukin 13 (IL-13) is a major effector molecule for T-helper type 2 inflammation and is pathogenic in allergic diseases such as asthma. The effects of IL-13 are mediated via a pathway that is initiated by binding to a heterodimeric receptor consisting of IL-13Rα1 and IL-4Rα. Antibodies raised against IL-13 can block its inflammatory effects by interfering with binding to either of the two receptor polypeptides. Lebrikizumab is a monoclonal anti-IL-13 antibody that has shown clinical benefit in a phase II study for the treatment of moderate-to-severe uncontrolled asthma. Here we report the molecular structure of IL-13 in complex with the Fab from lebrikizumab by X-ray crystallography at 1.9Å resolution. We show that lebrikizumab inhibits IL-13 signaling by binding to IL-13 with very high affinity and blocking IL-13 binding to IL-4Rα. In addition, we use site-directed mutations to identify the most important antibody contributors to binding. Our studies define key features of lebrikizumab binding and its mechanism of action that may contribute to its clinical effects. PubMed: 23357170DOI: 10.1016/j.jmb.2013.01.024 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.9 Å) |
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