9ETH

Complex structure of IL-36R D1-D2 domain with 36R-P192 and BI655130 Fab

これはPDB形式変換不可エントリーです。

9ETH の概要

• エントリーDOI: 10.2210/pdb9eth/pdb
• 分子名称: BI00655130 Fab heavy chain, GLYCEROL, BI00655130 Fab light chain, ... (11 entities in total)
• 機能のキーワード: inhibitor, complex, fab, cytokine
• 由来する生物種: Homo sapiens; 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 75736.13

構造登録者

Scheufler, C.,Wirth, E.,Lehmann, S. (登録日: 2024-03-26, 公開日: 2025-02-26)

主引用文献

Velcicky, J.,Cremosnik, G.,Scheufler, C.,Meier, P.,Wirth, E.,Felber, R.,Ramage, P.,Schaefer, M.,Kaiser, C.,Lehmann, S.,Kutil, R.,Singeisen, S.,Mueller-Ristig, D.,Popp, S.,Cebe, R.,Lehr, P.,Kaupmann, K.,Erbel, P.,Rohn, T.A.,Giovannoni, J.,Dumelin, C.E.,Martiny-Baron, G.
Discovery of selective low molecular weight interleukin-36 receptor antagonists by encoded library technologies.
Nat Commun, 16:1669-1669, 2025

PubMed Abstract: Interleukin-36 receptor (IL-36R), belonging to the IL-1 receptor family, is crucial for host defense and tissue repair. Targeting cytokine receptors with low molecular weight (LMW) compounds remains challenging due to their interaction with the large surface area of cytokine. In this study, two encoded library technologies are used to identify LMW molecules binding to IL-36R's extracellular domain. The mRNA-based display technique identifies 36R-P138, a macrocyclic peptide blocking IL-36R signaling. Importantly, its optimized analog (36R-P192) also effectively suppresses expression of marker genes induced by IL-36 in human skin biopsies. DNA encoded libraries (DEL) screening delivers 36R-D481, a high affinity LMW IL-36R binder, effectively inhibiting IL-36 signaling. X-ray crystallography analysis reveals that both the cyclic peptide and DEL-compound bind to the IL-36R's D1 domain, potentially disrupting IL-36 cytokine binding. This study demonstrates that it is possible to target a cytokine receptor within the IL-1 receptor family using a small molecule ( < 1000 Da).

PubMed: 39955284
DOI: 10.1038/s41467-025-56601-7

実験手法

X-RAY DIFFRACTION (2.3 Å)