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4I77

Lebrikizumab Fab bound to IL-13

4I77 の概要
エントリーDOI10.2210/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
Eigenbrot, C.,Ultsch, M. (登録日: 2012-11-30, 公開日: 2013-02-06, 最終更新日: 2024-10-09)
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: 23357170
DOI: 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)
構造検証レポート
Validation report summary of 4i77
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2026-02-04に公開中

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