8G4Y
Structure of ZNRF3 ECD bound to peptide MK1-3.6.10
8G4Y の概要
| エントリーDOI | 10.2210/pdb8g4y/pdb |
| 分子名称 | E3 ubiquitin-protein ligase ZNRF3, MK1-3.6.10 (3 entities in total) |
| 機能のキーワード | ubiquitin ligase, wnt signal, cell surface, ckp, ligase |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 24162.19 |
| 構造登録者 | |
| 主引用文献 | Kschonsak, Y.T.,Gao, X.,Miller, S.E.,Hwang, S.,Marei, H.,Wu, P.,Li, Y.,Ruiz, K.,Dorighi, K.,Holokai, L.,Perampalam, P.,Tsai, W.K.,Kee, Y.S.,Agard, N.J.,Harris, S.F.,Hannoush, R.N.,de Sousa E Melo, F. Potent and selective binders of the E3 ubiquitin ligase ZNRF3 stimulate Wnt signaling and intestinal organoid growth. Cell Chem Biol, 31:1176-, 2024 Cited by PubMed Abstract: Selective and precise activation of signaling transduction cascades is key for cellular reprogramming and tissue regeneration. However, the development of small- or large-molecule agonists for many signaling pathways has remained elusive and is rate limiting to realize the full clinical potential of regenerative medicine. Focusing on the Wnt pathway, here we describe a series of disulfide-constrained peptides (DCPs) that promote Wnt signaling activity by modulating the cell surface levels of ZNRF3, an E3 ubiquitin ligase that controls the abundance of the Wnt receptor complex FZD/LRP at the plasma membrane. Mechanistically, monomeric DCPs induce ZNRF3 ubiquitination, leading to its cell surface clearance, ultimately resulting in FZD stabilization. Furthermore, we engineered multimeric DCPs that induce expansive growth of human intestinal organoids, revealing a dependence between valency and ZNRF3 clearance. Our work highlights a strategy for the development of potent, biologically active Wnt signaling pathway agonists via targeting of ZNRF3. PubMed: 38056465DOI: 10.1016/j.chembiol.2023.11.006 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.41 Å) |
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