Abstract
Molecular glues powerfully control protein proximity but have largely eluded direct screening. A promising avenue for addressing this challenge lies within pinpointing the fundamental features for function-first identification of molecular gluing events. In the widely accepted mechanism, a molecular glue stabilizes two proteins within a ternary complex─here, we show how differences in affinity for ternary and binary complexes directly categorize glues from nonglues. We leverage these differences together with high-throughput chemical synthesis and affinity-selection mass-spectrometry to discover a molecular glue from a suite of over 20,000 crude chemical reaction mixtures. Orthogonal assays robustly support the identification of molecular glues via ternary complex stability. Our findings suggest that a roadmap for de novo molecular glue discovery lies within kinetic profiling of unpurified mixtures of small organic molecules against protein pairs.
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CITATION STYLE
Hu, M., Ochoada, J., Actis, M., McGowan, K., Jarusiewicz, J. A., Yoshimura, S., … Blair, D. J. (2026). Direct-to-Biology Enabled Molecular Glue Discovery. Journal of the American Chemical Society, 148(1), 20–27. https://doi.org/10.1021/jacs.5c13496
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