8TRS

Structure of the EphA2 CRD bound to FabS1CE_C1, trigonal form

8TRS の概要

• エントリーDOI: 10.2210/pdb8trs/pdb
• 関連するPDBエントリー: 8TRS 8TRT 8TRV
• 分子名称: S1CE variant of Fab C1 heavy chain, S1CE variant of Fab C1 light chain, Ephrin type-A receptor 2, ... (8 entities in total)
• 機能のキーワード: cell signalling, antibody, agonist, high affinity, clustering, activation, signaling protein-immune system complex, signaling protein/immune system
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 63826.23

構造登録者

Singer, A.U.,Bruce, H.A.,Blazer, L.,Adams, J.J.,Sicheri, F.,Sidhu, S.S. (登録日: 2023-08-10, 公開日: 2023-11-22, 最終更新日: 2024-11-13)

主引用文献

Bruce, H.A.,Singer, A.U.,Filippova, E.V.,Blazer, L.L.,Adams, J.J.,Enderle, L.,Ben-David, M.,Radley, E.H.,Mao, D.Y.L.,Pau, V.,Orlicky, S.,Sicheri, F.,Kurinov, I.,Atwell, S.,Kossiakoff, A.A.,Sidhu, S.S.
Engineered antigen-binding fragments for enhanced crystallization of antibody:antigen complexes.
Protein Sci., 33:e4824-e4824, 2024

PubMed Abstract: The atomic-resolution structural information that X-ray crystallography can provide on the binding interface between a Fab and its cognate antigen is highly valuable for understanding the mechanism of interaction. However, many Fab:antigen complexes are recalcitrant to crystallization, making the endeavor a considerable effort with no guarantee of success. Consequently, there have been significant steps taken to increase the likelihood of Fab:antigen complex crystallization by altering the Fab framework. In this investigation, we applied the surface entropy reduction strategy coupled with phage-display technology to identify a set of surface substitutions that improve the propensity of a human Fab framework to crystallize. In addition, we showed that combining these surface substitutions with previously reported Crystal Kappa and elbow substitutions results in an extraordinary improvement in Fab and Fab:antigen complex crystallizability, revealing a strong synergistic relationship between these sets of substitutions. Through comprehensive Fab and Fab:antigen complex crystallization screenings followed by structure determination and analysis, we defined the roles that each of these substitutions play in facilitating crystallization and how they complement each other in the process.

PubMed: 37945533
DOI: 10.1002/pro.4824

実験手法

X-RAY DIFFRACTION (1.9 Å)