Lin, H.; Yu, X.; Zheng, H.; Che, X.; Wang, J.

This study reports the discovery and characterization of novel CRBN molecular glues that selectively induce the proteasomal degradation of the hematopoietic-specific signaling protein VAV1, a key target in hematological malignancies and autoimmune diseases. Utilizing unbiased global proteomics, we identified phenyl-glutarimide derivatives NGT-201-12, as effective VAV1 degraders, with its C-terminal SH3 domain (SH32) being crucial for this interaction. A significant finding is the elucidation of a non-canonical RT-loop degron (RDxS motif, residues 796-799) within VAV1 SH32, distinct from previously characterized G-loop degrons. This discovery, supported by advanced computational modeling using the YDS-GlueFold platform and validated by site-directed mutagenesis, highlights versatility of CRBN in recognizing diverse neosubstrate motifs.