6V1A
immune receptor complex
6V1A の概要
| エントリーDOI | 10.2210/pdb6v1a/pdb |
| 関連するPDBエントリー | 6V0Y 6V13 6V15 6V18 6V19 |
| 分子名称 | HLA class II histocompatibility antigen, DR alpha chain, HLA class II histocompatibility antigen, DRB1-4 beta chain, Fibrinogen beta 74cit69-81, ... (9 entities in total) |
| 機能のキーワード | immune receptor, immune system |
| 由来する生物種 | Homo sapiens (Human) 詳細 |
| タンパク質・核酸の鎖数 | 5 |
| 化学式量合計 | 99302.02 |
| 構造登録者 | |
| 主引用文献 | Lim, J.J.,Jones, C.M.,Loh, T.J.,Ting, Y.T.,Zareie, P.,Loh, K.L.,Felix, N.J.,Suri, A.,McKinnon, M.,Stevenaert, F.,Sharma, R.K.,Klareskog, L.,Malmstrom, V.,Baker, D.G.,Purcell, A.W.,Reid, H.H.,La Gruta, N.L.,Rossjohn, J. The shared susceptibility epitope of HLA-DR4 binds citrullinated self-antigens and the TCR. Sci Immunol, 6:-, 2021 Cited by PubMed Abstract: Individuals expressing HLA-DR4 bearing the shared susceptibility epitope (SE) have an increased risk of developing rheumatoid arthritis (RA). Posttranslational modification of self-proteins via citrullination leads to the formation of neoantigens that can be presented by HLA-DR4 SE allomorphs. However, in T cell-mediated autoimmunity, the interplay between the HLA molecule, posttranslationally modified epitope(s), and the responding T cell repertoire remains unclear. In HLA-DR4 transgenic mice, we show that immunization with a Fibβ-74cit peptide led to a population of HLA-DR4 tetramer T cells that exhibited biased T cell receptor (TCR) β chain usage, which was attributable to selective clonal expansion from the preimmune repertoire. Crystal structures of pre- and postimmune TCRs showed that the SE of HLA-DR4 represented a main TCR contact zone. Immunization with a double citrullinated epitope (Fibβ-72,74cit) altered the responding HLA-DR4 tetramer T cell repertoire, which was due to the P2-citrulline residue interacting with the TCR itself. We show that the SE of HLA-DR4 has dual functionality, namely, presentation and a direct TCR recognition determinant. Analogous biased TCR β chain usage toward the Fibβ-74cit peptide was observed in healthy HLA-DR4 individuals and patients with HLA-DR4 RA, thereby suggesting a link to human RA. PubMed: 33863750DOI: 10.1126/sciimmunol.abe0896 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.29 Å) |
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