6HMT

Ternary complex of Estrogen Receptor alpha peptide and 14-3-3 sigma C42 mutant bound to disulfide fragment PPI stabilizer 2

6HMT の概要

• エントリーDOI: 10.2210/pdb6hmt/pdb
• 分子名称: 14-3-3 protein sigma, Estrogen Receptor, MAGNESIUM ION, ... (5 entities in total)
• 機能のキーワード: protein-protein interaction, fragment, tethering, stabilizer, protein binding
• 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: 27711.84

構造登録者

Sijbesma, E.,Hallenbeck, K.K.,Leysen, S.,Arkin, M.R.,Ottmann, C. (登録日: 2018-09-12, 公開日: 2019-02-27, 最終更新日: 2024-11-20)

主引用文献

Sijbesma, E.,Hallenbeck, K.K.,Leysen, S.,de Vink, P.J.,Skora, L.,Jahnke, W.,Brunsveld, L.,Arkin, M.R.,Ottmann, C.
Site-Directed Fragment-Based Screening for the Discovery of Protein-Protein Interaction Stabilizers.
J. Am. Chem. Soc., 141:3524-3531, 2019

PubMed Abstract: Modulation of protein-protein interactions (PPIs) by small molecules has emerged as a valuable approach in drug discovery. Compared to direct inhibition, PPI stabilization is vastly underexplored but has strong advantages, including the ability to gain selectivity by targeting an interface formed only upon association of proteins. Here, we present the application of a site-directed screening technique based on disulfide trapping (tethering) to select for fragments that enhance the affinity between protein partners. We target the phosphorylation-dependent interaction between the hub protein 14-3-3σ and a peptide derived from Estrogen Receptor α (ERα), an important breast cancer target that is negatively regulated by 14-3-3σ. We identify orthosteric stabilizers that increase 14-3-3/ERα affinity up to 40-fold and propose the mechanism of stabilization based on X-ray crystal structures. These fragments already display partial selectivity toward ERα-like motifs over other representative 14-3-3 clients. This first of its kind study illustrates the potential of the tethering approach to overcome the hurdles in systematic PPI stabilizer discovery.

PubMed: 30707565
DOI: 10.1021/jacs.8b11658

実験手法

X-RAY DIFFRACTION (1.1 Å)