7STZ

Crystal Structure of Human E-cadherin EC1-5 bound by mouse monoclonal antibody Fab mAb-1_19A11

7STZ の概要

• エントリーDOI: 10.2210/pdb7stz/pdb
• 分子名称: Cadherin-1, mAb-1_19A11 Heavy Chain, mAb-1_19A11 Light Chain, ... (10 entities in total)
• 機能のキーワード: ssgcid, cadherin-1, cell adhesion, structural genomics, seattle structural genomics center for infectious disease, cell adhesion-immune system complex, cell adhesion/immune system
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 6
• 化学式量合計: 239278.42

構造登録者

Seattle Structural Genomics Center for Infectious Disease,Seattle Structural Genomics Center for Infectious Disease (SSGCID) (登録日: 2021-11-15, 公開日: 2022-01-26, 最終更新日: 2024-11-06)

主引用文献

Maker, A.,Bolejack, M.,Schecterson, L.,Hammerson, B.,Abendroth, J.,Edwards, T.E.,Staker, B.,Myler, P.J.,Gumbiner, B.M.
Regulation of multiple dimeric states of E-cadherin by adhesion activating antibodies revealed through Cryo-EM and X-ray crystallography.
Pnas Nexus, 1:pgac163-pgac163, 2022

PubMed Abstract: E-cadherin adhesion is regulated at the cell surface, a process that can be replicated by activating antibodies. We use cryo-electron microscopy (EM) and X-ray crystallography to examine functional states of the cadherin adhesive dimer. This dimer is mediated by N-terminal beta strand-swapping involving Trp2, and forms via a different transient X-dimer intermediate. X-dimers are observed in cryo-EM along with monomers and strand-swap dimers, indicating that X-dimers form stable interactions. A novel EC4-mediated dimer was also observed. Activating Fab binding caused no gross structural changes in E-cadherin monomers, but can facilitate strand swapping. Moreover, activating Fab binding is incompatible with the formation of the X-dimer. Both cryo-EM and X-ray crystallography reveal a distinctive twisted strand-swap dimer conformation caused by an outward shift in the N-terminal beta strand that may represent a strengthened state. Thus, regulation of adhesion involves changes in cadherin dimer configurations.

PubMed: 36157596
DOI: 10.1093/pnasnexus/pgac163

実験手法

X-RAY DIFFRACTION (2.95 Å)