5Y9J
BAFF in complex with belimumab
5Y9J の概要
エントリーDOI | 10.2210/pdb5y9j/pdb |
分子名称 | belibumab light chain, belimumab heavy chain, Tumor necrosis factor ligand superfamily member 13B, ... (4 entities in total) |
機能のキーワード | baff, belimumab, antibody, lupus, protein binding |
由来する生物種 | Homo sapiens 詳細 |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 64803.42 |
構造登録者 | |
主引用文献 | Shin, W.,Lee, H.T.,Lim, H.,Lee, S.H.,Son, J.Y.,Lee, J.U.,Yoo, K.Y.,Ryu, S.E.,Rhie, J.,Lee, J.Y.,Heo, Y.S. BAFF-neutralizing interaction of belimumab related to its therapeutic efficacy for treating systemic lupus erythematosus. Nat Commun, 9:1200-1200, 2018 Cited by PubMed Abstract: BAFF, a member of the TNF superfamily, has been recognized as a good target for autoimmune diseases. Belimumab, an anti-BAFF monoclonal antibody, was approved by the FDA for use in treating systemic lupus erythematosus. However, the molecular basis of BAFF neutralization by belimumab remains unclear. Here our crystal structure of the BAFF-belimumab Fab complex shows the precise epitope and the BAFF-neutralizing mechanism of belimumab, and demonstrates that the therapeutic activity of belimumab involves not only antagonizing the BAFF-receptor interaction, but also disrupting the formation of the more active BAFF 60-mer to favor the induction of the less active BAFF trimer through interaction with the flap region of BAFF. In addition, the belimumab HCDR3 loop mimics the DxL(V/L) motif of BAFF receptors, thereby binding to BAFF in a similar manner as endogenous BAFF receptors. Our data thus provides insights for the design of new drugs targeting BAFF for the treatment of autoimmune diseases. PubMed: 29572471DOI: 10.1038/s41467-018-03620-2 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.05 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