Baek Kheewoong, Metivier Rebecca J, Roy Burman Shourya S, Bushman Jonathan W, Yoon Hojong, Lumpkin Ryan J, Ryan Julia K, Abeja Dinah M, Lakshminarayan Megha, Yue Hong, Ojeda Samuel, Xiong Yuan, Che Jianwei, Verano Alyssa L, Schmoker Anna M, Gray Nathanael S, Donovan Katherine A, Fischer Eric S
Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts, USA.
Nat Commun. 2025 Jul 24;16(1):6831. doi: 10.1038/s41467-025-62099-w.
Induced proximity by molecular glues refers to strategies that leverage the recruitment of proteins to facilitate their modification, regulation or degradation. As prospective design of molecular glues remains challenging, unbiased discovery methods are necessary to discover new chemical targets. Here we establish a high throughput affinity proteomics workflow leveraging E3 ligase activity-impaired CRBN-DDB1ΔB in cell lysates for the unbiased identification of molecular glue targets. By mapping the interaction landscape of CRBN-binding molecular glues, we unveil 298 protein targets and demonstrate the utility of enrichment methods for identifying targets overlooked by established methods. We use a computational workflow to estimate target confidence and perform biochemical and structural validation of uncharacterized neo-substrates. We further identify a lead compound for the previously untargeted non-zinc finger PPIL4 through a biochemical screen. Our study provides a comprehensive inventory of targets chemically recruited to CRBN and delivers a robust and scalable workflow for identifying drug-induced protein interactions in cell lysates.
分子胶诱导邻近效应是指利用蛋白质招募来促进其修饰、调节或降解的策略。由于分子胶的前瞻性设计仍然具有挑战性,因此需要无偏向性的发现方法来发现新的化学靶点。在此,我们建立了一种高通量亲和蛋白质组学工作流程,利用细胞裂解物中E3连接酶活性受损的CRBN-DDB1ΔB来无偏向性地鉴定分子胶靶点。通过绘制与CRBN结合的分子胶的相互作用图谱,我们揭示了298个蛋白质靶点,并证明了富集方法在识别现有方法遗漏的靶点方面的效用。我们使用计算工作流程来估计靶点可信度,并对未表征的新底物进行生化和结构验证。我们还通过生化筛选为之前未靶向的非锌指蛋白PPIL4确定了一种先导化合物。我们的研究提供了一份化学招募到CRBN的靶点的综合清单,并提供了一种强大且可扩展的工作流程,用于识别细胞裂解物中药物诱导的蛋白质相互作用。