3SGE
Crystal structure of mAb 17.2 in complex with R13 peptide
3SGE の概要
| エントリーDOI | 10.2210/pdb3sge/pdb |
| 関連するPDBエントリー | 3SGD |
| 分子名称 | Light Chain, Heavy Chain, R13 peptide, ... (5 entities in total) |
| 機能のキーワード | immunoglobulin, antigen binding, immune system |
| 由来する生物種 | Mus musculus (mouse) 詳細 |
| タンパク質・核酸の鎖数 | 6 |
| 化学式量合計 | 98546.02 |
| 構造登録者 | Pizarro, J.C.,Boulot, G.,Hontebeyrie, M.,Bentley, G.A. (登録日: 2011-06-14, 公開日: 2011-11-09, 最終更新日: 2024-11-27) |
| 主引用文献 | Pizarro, J.C.,Boulot, G.,Bentley, G.A.,Gomez, K.A.,Hoebeke, J.,Hontebeyrie, M.,Levin, M.J.,Smulski, C.R. Crystal structure of the complex mAb 17.2 and the C-terminal region of Trypanosoma cruzi P2 Beta protein: implications in cross-reactivity Plos Negl Trop Dis, 5:e1375-e1375, 2011 Cited by PubMed Abstract: Patients with Chronic Chagas' Heart Disease possess high levels of antibodies against the carboxyl-terminal end of the ribosomal P2ß protein of Trypanosoma cruzi (TcP2ß). These antibodies, as well as the murine monoclonal antibody (mAb) 17.2, recognize the last 13 amino acids of TcP2ß (called the R13 epitope: EEEDDDMGFGLFD) and are able to cross-react with, and stimulate, the ß1 adrenergic receptor (ß1-AR). Indeed, the mAb 17.2 was able to specifically detect human β1-AR, stably transfected into HEK cells, by flow cytometry and to induce repolarisation abnormalities and first degree atrioventricular conduction block after passive transfer to naïve mice. To study the structural basis of this cross-reactivity, we determined the crystal structure of the Fab region of the mAb 17.2 alone at 2.31 Å resolution and in complex with the R13 peptide at 1.89 Å resolution. We identified as key contact residues on R13 peptide Glu3, Asp6 and Phe9 as was previously shown by alanine scanning. Additionally, we generated a model of human β1-AR to elucidate the interaction with anti-R13 antibodies. These data provide an understanding of the molecular basis of cross-reactive antibodies induced by chronic infection with Trypanosoma cruzi. PubMed: 22069505DOI: 10.1371/journal.pntd.0001375 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.89 Å) |
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