7VF3

Plexin B1 extracellular fragment in complex with lasso-grafted PB1m7 peptide

7VF3 の概要

• エントリーDOI: 10.2210/pdb7vf3/pdb
• 分子名称: Plexin-B1, Uteroglobin,PB1m7 peptide,Uteroglobin, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (7 entities in total)
• 機能のキーワード: plexin, complex, signaling protein
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 149752.42

構造登録者

Sugano, N.N.,Hirata, K.,Yamashita, K.,Yamamoto, M.,Arimori, T.,Takagi, J. (登録日: 2021-09-10, 公開日: 2022-08-17, 最終更新日: 2024-11-20)

主引用文献

Sugano-Nakamura, N.,Matoba, K.,Hirose, M.,Bashiruddin, N.K.,Matsunaga, Y.,Yamashita, K.,Hirata, K.,Yamamoto, M.,Arimori, T.,Suga, H.,Takagi, J.
De novo Fc-based receptor dimerizers differentially modulate PlexinB1 function.
Structure, 30:1411-1423.e4, 2022

PubMed Abstract: Signaling by single-pass transmembrane receptors often involves a formation of ligand-induced receptor dimers with particular conformation, and bivalent receptor binders can modulate receptor functions by inducing different receptor dimer conformations, although such agents are difficult to design. Here, we describe the generation of both antagonistic and agonistic receptor dimerizers toward PlexinB1 (PlxnB1), a receptor for semaphorin 4D (Sema4D), by grafting two different PlxnB1-binding peptides onto the human immunoglobulin G1 (IgG1) Fc protein. The function-modulating activity of a peptide Fc was strongly dependent on the type of the peptide as well as the grafting site, with the best variants showing activity at an nM concentration range. Structural analysis of each peptide-PlxnB1 complex revealed that the agonistic Fc dimerizes PlxnB1 in a face-to-face fashion similar to that induced by Sema4D, whereas antagonistic Fc would induce signaling-incompetent PlxnB1 dimer conformation, enforcing the idea that plexin activation is primarily controlled by the receptor orientation within the dimer.

PubMed: 35981535
DOI: 10.1016/j.str.2022.07.008

実験手法

X-RAY DIFFRACTION (2.29 Å)