3GJF
Rational development of high-affinity T-cell receptor-like antibodies
3GJF の概要
エントリーDOI | 10.2210/pdb3gjf/pdb |
関連するPDBエントリー | 3GJE 3GJG |
分子名称 | HLA class I histocompatibility antigen, A-2 alpha chain, Beta-2-microglobulin, NYESO-1 peptide, ... (6 entities in total) |
機能のキーワード | mhc, antibody, disulfide bond, glycoprotein, host-virus interaction, immune response, membrane, mhc i, phosphoprotein, polymorphism, transmembrane, ubl conjugation, disease mutation, glycation, immunoglobulin domain, pyrrolidone carboxylic acid, secreted, immune system |
由来する生物種 | Homo sapiens (human) 詳細 |
細胞内の位置 | Membrane; Single-pass type I membrane protein: P01892 Secreted: P61769 |
タンパク質・核酸の鎖数 | 10 |
化学式量合計 | 181421.65 |
構造登録者 | Stewart-Jones, G.,Wadle, A.,Hombach, A.,Shenderov, E.,Held, G.,Fischer, E.,Kleber, S.,Stenner-Liewen, F.,Bauer, S.,McMichael, A.,Knuth, A.,Abken, H.,Hombach, A.A.,Cerundolo, V.,Jones, E.Y.,Renner, C. (登録日: 2009-03-08, 公開日: 2009-04-28, 最終更新日: 2024-11-06) |
主引用文献 | Stewart-Jones, G.,Wadle, A.,Hombach, A.,Shenderov, E.,Held, G.,Fischer, E.,Kleber, S.,Stenner-Liewen, F.,Bauer, S.,McMichael, A.,Knuth, A.,Abken, H.,Hombach, A.A.,Cerundolo, V.,Jones, E.Y.,Renner, C. Rational development of high-affinity T-cell receptor-like antibodies Proc.Natl.Acad.Sci.USA, 106:5784-5788, 2009 Cited by PubMed Abstract: T-cell interaction with a target cell is a key event in the adaptive immune response and primarily driven by T-cell receptor (TCR) recognition of peptide-MHC (pMHC) complexes. TCR avidity for a given pMHC is determined by number of MHC molecules, availability of coreceptors, and TCR affinity for MHC or peptide, respectively, with peptide recognition being the most important factor to confer target specificity. Here we present high-resolution crystal structures of 2 Fab antibodies in complex with the immunodominant NY-ESO-1(157-165) peptide analogue (SLLMWITQV) presented by HLA-A*0201 and compare them with a TCR recognizing the same pMHC. Binding to the central methionine-tryptophan peptide motif and orientation of binding were almost identical for Fabs and TCR. As the MW "peg" dominates the contacts between Fab and peptide, we estimated the contributions of individual amino acids between the Fab and peptide to provide the rational basis for a peptide-focused second-generation, high-affinity antibody library. The final Fab candidate achieved better peptide binding by 2 light-chain mutations, giving a 20-fold affinity improvement to 2-4 nM, exceeding the affinity of the TCR by 1,000-fold. The high-affinity Fab when grafted as recombinant TCR on T cells conferred specific killing of HLA-A*0201/NY-ESO-1(157-165) target cells. In summary, we prove that affinity maturation of antibodies mimicking a TCR is possible and provide a strategy for engineering high-affinity antibodies that can be used in targeting specific pMHC complexes for diagnostic and therapeutic purposes. PubMed: 19307587DOI: 10.1073/pnas.0901425106 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.9 Å) |
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