8GOP
SARS-CoV-2 specific private TCR RLQ7
8GOP の概要
エントリーDOI | 10.2210/pdb8gop/pdb |
分子名称 | SARS-CoV-2 specific private TCR RLQ7 beta, SARS-CoV-2 specific private TCR RLQ7 alpha (3 entities in total) |
機能のキーワード | sars-cov-2, private tcr, tcr-p-hla, immune system |
由来する生物種 | Homo sapiens 詳細 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 51087.84 |
構造登録者 | |
主引用文献 | Wu, D.,Efimov, G.A.,Bogolyubova, A.V.,Pierce, B.G.,Mariuzza, R.A. Structural insights into protection against a SARS-CoV-2 spike variant by T cell receptor (TCR) diversity. J.Biol.Chem., 299:103035-103035, 2023 Cited by PubMed Abstract: T cells play a crucial role in combatting SARS-CoV-2 and forming long-term memory responses to this coronavirus. The emergence of SARS-CoV-2 variants that can evade T cell immunity has raised concerns about vaccine efficacy and the risk of reinfection. Some SARS-CoV-2 T cell epitopes elicit clonally restricted CD8 T cell responses characterized by T cell receptors (TCRs) that lack structural diversity. Mutations in such epitopes can lead to loss of recognition by most T cells specific for that epitope, facilitating viral escape. Here, we studied an HLA-A2-restricted spike protein epitope (RLQ) that elicits CD8 T cell responses in COVID-19 convalescent patients characterized by highly diverse TCRs. We previously reported the structure of an RLQ-specific TCR (RLQ3) with greatly reduced recognition of the most common natural variant of the RLQ epitope (T1006I). Opposite to RLQ3, TCR RLQ7 recognizes T1006I with even higher functional avidity than the WT epitope. To explain the ability of RLQ7, but not RLQ3, to tolerate the T1006I mutation, we determined structures of RLQ7 bound to RLQ-HLA-A2 and T1006I-HLA-A2. These complexes show that there are multiple structural solutions to recognizing RLQ and thereby generating a clonally diverse T cell response to this epitope that assures protection against viral escape and T cell clonal loss. PubMed: 36806685DOI: 10.1016/j.jbc.2023.103035 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.8 Å) |
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