Discovery of Novel Inhibitors for WD Repeat-Containing Protein 5 (WDR5)-MYC Protein–Protein Interaction

IF 3.2 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Wei Sun, Huaxing Yu, Jiuyong Ye, Luoheng Qin, Linli Wang, Hailu Yan, Zhimin Zhang, Alex Aliper, Feng Ren, Xiao Ding, Alex Zhavoronkov, Dongzhou Liu
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引用次数: 0

Abstract

The WD Repeat-Containing Protein 5 (WDR5) and MYC interaction is crucial for MYC-mediated oncogenesis, yet effective therapeutic intervention remains challenging due to the limited efficacy of current treatments targeting WDR5. Herein, we report the discovery of novel WDR5-MYC protein–protein interaction (PPI) inhibitors with improved potency and drug-like properties by utilizing a generative chemistry platform along with a physics-model-based tool AlChemistry. Initially, three hits were identified with reasonable binding affinity for WDR5, and further refinement through detailed structural analysis led to the discovery of sub-micromolar affinity compounds (compound 9c-1), which are > 30-fold better than reported inhibitors. These findings provide a promising starting point for targeting the WDR5-MYC interaction in MYC-driven cancers.

WDR5 -MYC蛋白相互作用新抑制剂的发现
WDR5和MYC的相互作用对于MYC介导的肿瘤发生至关重要,但由于目前针对WDR5的治疗效果有限,有效的治疗干预仍然具有挑战性。在此,我们报告了利用生成化学平台和基于物理模型的工具AlChemistry,发现了新的WDR5-MYC蛋白-蛋白相互作用(PPI)抑制剂,具有改善的效力和药物样特性。最初,我们确定了三个与WDR5具有合理结合亲和力的hit,通过详细的结构分析进一步细化,发现了亚微摩尔亲和力化合物(化合物9c-1),其效果比报道的抑制剂好30倍。这些发现为在myc驱动的癌症中靶向WDR5-MYC相互作用提供了一个有希望的起点。
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来源期刊
Chemical Biology & Drug Design
Chemical Biology & Drug Design 医学-生化与分子生物学
CiteScore
5.10
自引率
3.30%
发文量
164
审稿时长
4.4 months
期刊介绍: Chemical Biology & Drug Design is a peer-reviewed scientific journal that is dedicated to the advancement of innovative science, technology and medicine with a focus on the multidisciplinary fields of chemical biology and drug design. It is the aim of Chemical Biology & Drug Design to capture significant research and drug discovery that highlights new concepts, insight and new findings within the scope of chemical biology and drug design.
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