Structural Genomics Consortium, University of Toronto, Ontario M5G 1L7, Canada.
Google Research, Mountain View, California 94043, United States.
J Med Chem. 2023 Dec 14;66(23):16051-16061. doi: 10.1021/acs.jmedchem.3c01471. Epub 2023 Nov 23.
WD40 repeat-containing protein 91 (WDR91) regulates early-to-late endosome conversion and plays vital roles in endosome fusion, recycling, and transport. WDR91 was recently identified as a potential host factor for viral infection. We employed DNA-encoded chemical library (DEL) selection against the WDR domain of WDR91, followed by machine learning to predict ligands from the synthetically accessible Enamine REAL database. Screening of predicted compounds identified a WDR91 selective compound , with a of 6 ± 2 μM by surface plasmon resonance. The co-crystal structure confirmed the binding of to the WDR91 side pocket, in proximity to cysteine 487, which led to the discovery of covalent analogues and . The covalent adduct formation for and was confirmed by intact mass liquid chromatography-mass spectrometry. The discovery of , , and , accompanying structure-activity relationship, and the co-crystal structures provide valuable insights for designing potent and selective chemical tools against WDR91 to evaluate its therapeutic potential.
WD40 重复蛋白 91(WDR91)调节早期至晚期内体转化,在促进内体融合、回收和运输方面发挥着重要作用。WDR91 最近被鉴定为一种潜在的病毒感染宿主因子。我们采用针对 WDR91 的 WDR 结构域的 DNA 编码化学文库(DEL)筛选,然后通过机器学习从可合成的 Enamine REAL 数据库中预测配体。从预测的化合物中筛选出一种 WDR91 选择性化合物,其表面等离子体共振的 IC50 值为 6 ± 2 μM。共晶结构证实了化合物与 WDR91 侧袋的结合,该侧袋靠近半胱氨酸 487,这导致了共价类似物和的发现。通过完整质量液相色谱-质谱法证实了化合物和的共价加合物形成。化合物的发现,以及伴随的构效关系和共晶结构,为设计针对 WDR91 的有效且选择性的化学工具提供了有价值的见解,以评估其治疗潜力。