4N1E
Structural evidence for antigen receptor evolution
4N1E の概要
エントリーDOI | 10.2210/pdb4n1e/pdb |
関連するPDBエントリー | 4N1C |
分子名称 | immunoglobulin variable light chain domain, Lysozyme C (3 entities in total) |
機能のキーワード | immunoglobulin light chain variable domain, antigen-receptor interaction, ig-fold, immune system-hydrolase complex, immune system/hydrolase |
由来する生物種 | Homo sapiens (human) 詳細 |
細胞内の位置 | Secreted: P00698 |
タンパク質・核酸の鎖数 | 12 |
化学式量合計 | 151581.00 |
構造登録者 | |
主引用文献 | Rouet, R.,Langley, D.B.,Schofield, P.,Christie, M.,Roome, B.,Porebski, B.T.,Buckle, A.M.,Clifton, B.E.,Jackson, C.J.,Stock, D.,Christ, D. Structural reconstruction of protein ancestry. Proc. Natl. Acad. Sci. U.S.A., 114:3897-3902, 2017 Cited by PubMed Abstract: Ancestral protein reconstruction allows the resurrection and characterization of ancient proteins based on computational analyses of sequences of modern-day proteins. Unfortunately, many protein families are highly divergent and not suitable for sequence-based reconstruction approaches. This limitation is exemplified by the antigen receptors of jawed vertebrates (B- and T-cell receptors), heterodimers formed by pairs of Ig domains. These receptors are believed to have evolved from an extinct homodimeric ancestor through a process of gene duplication and diversification; however molecular evidence has so far remained elusive. Here, we use a structural approach and laboratory evolution to reconstruct such molecules and characterize their interaction with antigen. High-resolution crystal structures of reconstructed homodimeric receptors in complex with hen-egg white lysozyme demonstrate how nanomolar affinity binding of asymmetrical antigen is enabled through selective recruitment and structural plasticity within the receptor-binding site. Our results provide structural evidence in support of long-held theories concerning the evolution of antigen receptors, and provide a blueprint for the experimental reconstruction of protein ancestry in the absence of phylogenetic evidence. PubMed: 28356519DOI: 10.1073/pnas.1613477114 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.23 Å) |
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