8BYC

fragment-linked stabilizer for ERa - 14-3-3 interaction (1075316)

8BYC の概要

• エントリーDOI: 10.2210/pdb8byc/pdb
• 分子名称: 14-3-3 protein sigma, ERalpha peptide, MAGNESIUM ION, ... (5 entities in total)
• 機能のキーワード: 14-3-3, era, fragment linking, stabilizatoin, structural protein
• 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: 27683.41

構造登録者

Visser, E.J.,Vandenboorn, E.M.F.,Ottmann, C. (登録日: 2022-12-12, 公開日: 2023-08-02, 最終更新日: 2023-09-13)

主引用文献

Visser, E.J.,Jaishankar, P.,Sijbesma, E.,Pennings, M.A.M.,Vandenboorn, E.M.F.,Guillory, X.,Neitz, R.J.,Morrow, J.,Dutta, S.,Renslo, A.R.,Brunsveld, L.,Arkin, M.R.,Ottmann, C.
From Tethered to Freestanding Stabilizers of 14-3-3 Protein-Protein Interactions through Fragment Linking.
Angew.Chem.Int.Ed.Engl., 62:e202308004-e202308004, 2023

PubMed Abstract: Small-molecule stabilization of protein-protein interactions (PPIs) is a promising strategy in chemical biology and drug discovery. However, the systematic discovery of PPI stabilizers remains a largely unmet challenge. Herein we report a fragment-linking approach targeting the interface of 14-3-3 and a peptide derived from the estrogen receptor alpha (ERα) protein. Two classes of fragments-a covalent and a noncovalent fragment-were co-crystallized and subsequently linked, resulting in a noncovalent hybrid molecule in which the original fragment interactions were largely conserved. Supported by 20 crystal structures, this initial hybrid molecule was further optimized, resulting in selective, 25-fold stabilization of the 14-3-3/ERα interaction. The high-resolution structures of both the single fragments, their co-crystal structures and those of the linked fragments document a feasible strategy to develop orthosteric PPI stabilizers by linking to an initial tethered fragment.

PubMed: 37455289
DOI: 10.1002/anie.202308004

実験手法

X-RAY DIFFRACTION (1.6 Å)