Proteomics

Dataset Information

0

An engineered Cereblon optimized for high throughput screening and molecular glue discovery


ABSTRACT: The majority of clinical degraders utilize an immunomodulatory imide drug (IMiD)-based derivative, that directs their target to the E3 ligase receptor Cereblon (CRBN), however, identification of IMiD molecular glue substrates has remained underexplored. To tackle this, we design human CRBN constructs which retain all features for ternary complex formation, whilst allowing generation of homogenous and cost-efficient expression in E.coli. Extensive profiling of the construct, shows it to be the “best of both worlds” in terms of binding activity and ease of production. We next designed the ‘Enamine focused IMiD library’ and demonstrated applicability of the construct to high-throughput screening, identifying binders with high potency, ligand efficiency and specificity. Finally, we adapt our construct for proof of principle glue screening approaches enabling IMiD cellular interactome determination. Coupled with our IMiD binding landscape, the methods described here should serve as valuable tools to assist discovery of next generation CRBN glues.

INSTRUMENT(S): timsTOF Pro 2, timsTOF HT

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Cell Culture

SUBMITTER: Eric Fischer  

LAB HEAD: Eric Fischer

PROVIDER: PXD057393 | Pride | 2024-12-06

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
esf4_7665_Slot2-1_1_2358.d.zip Other
esf4_7666_Slot2-2_1_2359.d.zip Other
esf4_7667_Slot2-3_1_2360.d.zip Other
esf4_7668_Slot2-4_1_2361.d.zip Other
esf4_7671_Slot2-7_1_2366.d.zip Other
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Publications


The majority of clinical degraders utilize an immunomodulatory imide drug (IMiD)-based derivative that directs their target to the E3 ligase receptor cereblon (CRBN); however, identification of IMiD molecular glue substrates has remained underexplored. To tackle this, we design human CRBN constructs, which retain all features for ternary complex formation, while allowing generation of homogenous and cost-efficient expression in E. coli. Extensive profiling of the construct shows it to be the "be  ...[more]

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