Authors
Bingqi Tong, Sunny A Tang, Yifan Deng, Zhihan Nan, Alison X Gao, Gregory A Michaud, Simone Bonazzi, Frédéric Berst, Frédéric J Zécri, Shuang Liu, William J Gibson, Stuart L Schreiber
Published in
Advanced science (Weinheim, Baden-Wurttemberg, Germany). Pages e77819. Sep 27, 2026. Epub Sep 27, 2026.
Abstract
Chemical-induced proximity, particularly via molecular glues, represents a rapidly advancing therapeutic paradigm. Expanding the scope of proximity-based therapeutics requires generalizable discovery platforms that can be easily tailored to diverse presenter proteins. Here, we report a versatile DNA-encoded library (DEL) strategy designed to identify highly cooperative chemical inducers of proximity (CIPs) for multiple presenter proteins. By leveraging a novel precursor library constructed via on-DNA strained allene cycloadditions, we generated three distinct CIP-DELs biased toward Cereblon (CRBN), VHL, and FKBP12. Screening the CRBN-focused library with BRD9 identified B67b, a novel compound that mediates ternary complex formation between CRBN and BRD9 with nanomolar potency and strong molecular glue-like cooperativity (α >300). B67b engages BRD9 in a CRBN-dependent manner, a characteristic of classical molecular glues, and its high cooperativity is driven by the synergistic contribution of all its structural and stereochemical components. This work establishes a scalable, generalizable framework for repurposing generic DELs into presenter-specific screening tools, offering a powerful approach to accelerate the discovery of CIP therapeutics for a broad range of targets.
PMID:
42801576
Bibliographic data and abstract were imported from PubMed on 28 Sep 2026.
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