7EA6
Crystal structure of TCR-017 ectodomain
7EA6 の概要
| エントリーDOI | 10.2210/pdb7ea6/pdb |
| 分子名称 | T cell receptor 017 alpha chain, T cell receptor 017 beta chain (3 entities in total) |
| 機能のキーワード | t cell receptor, immune system |
| 由来する生物種 | Homo sapiens 詳細 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 99304.53 |
| 構造登録者 | |
| 主引用文献 | Lu, X.,Hosono, Y.,Nagae, M.,Ishizuka, S.,Ishikawa, E.,Motooka, D.,Ozaki, Y.,Sax, N.,Maeda, Y.,Kato, Y.,Morita, T.,Shinnakasu, R.,Inoue, T.,Onodera, T.,Matsumura, T.,Shinkai, M.,Sato, T.,Nakamura, S.,Mori, S.,Kanda, T.,Nakayama, E.E.,Shioda, T.,Kurosaki, T.,Takeda, K.,Kumanogoh, A.,Arase, H.,Nakagami, H.,Yamashita, K.,Takahashi, Y.,Yamasaki, S. Identification of conserved SARS-CoV-2 spike epitopes that expand public cTfh clonotypes in mild COVID-19 patients. J.Exp.Med., 218:-, 2021 Cited by PubMed Abstract: Adaptive immunity is a fundamental component in controlling COVID-19. In this process, follicular helper T (Tfh) cells are a subset of CD4+ T cells that mediate the production of protective antibodies; however, the SARS-CoV-2 epitopes activating Tfh cells are not well characterized. Here, we identified and crystallized TCRs of public circulating Tfh (cTfh) clonotypes that are expanded in patients who have recovered from mild symptoms. These public clonotypes recognized the SARS-CoV-2 spike (S) epitopes conserved across emerging variants. The epitope of the most prevalent cTfh clonotype, S864-882, was presented by multiple HLAs and activated T cells in most healthy donors, suggesting that this S region is a universal T cell epitope useful for booster antigen. SARS-CoV-2-specific public cTfh clonotypes also cross-reacted with specific commensal bacteria. In this study, we identified conserved SARS-CoV-2 S epitopes that activate public cTfh clonotypes associated with mild symptoms. PubMed: 34647971DOI: 10.1084/jem.20211327 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.18000239315 Å) |
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