Cereblon induces G3BP2 neosubstrate degradation using molecular surface mimicry

Molecular glue degraders (MGDs) are small-molecule compounds that divert E3 ligases to degrade nonnatural substrates called neosubstrates. Clinically effective MGDs bind cereblon (CRBN), a substrate receptor of the Cullin 4-RING E3 ubiquitin ligase (CRL4<sup>CRBN</sup>), and recruit neosubstrates to an MGD-induced neosurface on the CRBN CULT domain through molecular mimicry of a natural CRBN degron. Here, we identify G3BP2 (Ras-GAP SH3 domain-binding protein 2), a neosubstrate that bypasses canonical interactions with CRBN by engaging an unconventional binding site on the CRBN LON domain. The ternary complex interface does not resemble known interactions with CRBN. Instead, CRBN leverages a preexisting protein-protein interaction (PPI) hotspot on the target protein by mimicking an endogenous binding partner of G3BP2. Our findings suggest that composite neosurfaces that mimic and stabilize the footprint of natural PPIs (in short, 'glueprints') could become a viable strategy for the rational expansion of the MGD target repertoire.

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Publication Details

Journal
Nature Structural & Molecular Biology
Published
2026-01-20
DOI
https://doi.org/10.1038/s41594-025-01738-8
Citations
2
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
44.47
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article

Cereblon induces G3BP2 neosubstrate degradation using molecular surface mimicry

Kevin J. Lumb, Bernhard Fasching, Amine Sadok, Pablo Gaínza et al.
2 citations
Nature Structural & Molecular Biology
Protein Degradation and Inhibitors
44.47
article

Cereblon induces G3BP2 neosubstrate degradation using molecular surface mimicry

Kevin J. Lumb, Bernhard Fasching, Amine Sadok, Pablo Gaínza, R.D. Bunker, Daric Wible, Débora Bonenfant, Ilaria Lamberto, Etienne J. Donckèle, L. Wiedmer, Vaïk Strande, David Lyon, Magnus W. Walter, Peter Trenh, Rohitha Sriramaratnam, Vladislav Zarayskiy, Sharon A. Townson, Gian Marco De Donatis, Samuel Gilberto, Ralph Tiedt, Stefano Annunziato, Anastasia C. Murthy, Mary Zlotosch, Bradley DeMarco, Michelle Matysik, Camille Staehly, Laura Schwander, Danielle Rocio de Souza Arns Steiner, Despina Kapsitidou, Joao Silva, Jennifer Tsai, Reinaldo Almeida, Raphael Lieberherr, Chao Quan, Elena Dolgikh, John C. Castle, Georg Petzold
article en
2 citations

Abstract

Molecular glue degraders (MGDs) are small-molecule compounds that divert E3 ligases to degrade nonnatural substrates called neosubstrates. Clinically effective MGDs bind cereblon (CRBN), a substrate receptor of the Cullin 4-RING E3 ubiquitin ligase (CRL4<sup>CRBN</sup>), and recruit neosubstrates to an MGD-induced neosurface on the CRBN CULT domain through molecular mimicry of a natural CRBN degron. Here, we identify G3BP2 (Ras-GAP SH3 domain-binding protein 2), a neosubstrate that bypasses canonical interactions with CRBN by engaging an unconventional binding site on the CRBN LON domain. The ternary complex interface does not resemble known interactions with CRBN. Instead, CRBN leverages a preexisting protein-protein interaction (PPI) hotspot on the target protein by mimicking an endogenous binding partner of G3BP2. Our findings suggest that composite neosurfaces that mimic and stabilize the footprint of natural PPIs (in short, 'glueprints') could become a viable strategy for the rational expansion of the MGD target repertoire.

Nature Structural & Molecular BiologyVol. 33(3)
Boston Latin Academy (US), Jnana Therapeutics (United States) (US), Montrose Center (US)
Openalex Percentile: Top 0%
Protein Degradation and Inhibitors
44.47
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