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Identification of an allosteric site on the E3 ligase adapter cereblon

ABSTRACT: Cereblon (CRBN) is the target of thalidomide derivatives that achieve therapeutic efficacy against some hematologic neoplasias by recruiting neosubstrates for degradation. Despite the intense investigation of orthosteric thalidomide derivatives, little is known about alternate binding sites on CRBN. Here, we report the discovery of an evolutionarily conserved cryptic allosteric binding site on CRBN. Small molecule SB-405483 binds the allosteric site to cooperatively enhance the binding of orthosteric ligands and alter their neosubstrate degradation profiles. A survey of over 100 orthosteric ligands and their degradation targets reveals trends in the classes of compounds and neosubstrates where degradation outcomes are enhanced or inhibited by SB-405483. Structural investigations provide a mechanistic basis for the effects of the allosteric ligand by shifting the conformational distribution of CRBNopen to a novel CRBNint and increasing the CRBNclosed state. The discovery of a cryptic allosteric binding site on CRBN that alters the functional effects of orthosteric ligands opens new directions with broad implications for improving the selectivity and efficacy of CRBN therapeutics.

INSTRUMENT(S):

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Blood Cell, Cell Culture

DISEASE(S): Acute Leukemia

SUBMITTER: Christina Woo

LAB HEAD: Christina Woo

PROVIDER: PXD067391 | Pride | 2025-11-10

REPOSITORIES: Pride

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			Action	DRS
	230519E_Vanessa_TMT_MS2_SAM116_2022isoforms_1.msf	Msf
	250304E_Vanessa_Dippon_SUB07258_TMT-ms2_FT1.raw	Raw
	250304E_Vanessa_Dippon_SUB07258_TMT-ms2_FT10.raw	Raw
	250304E_Vanessa_Dippon_SUB07258_TMT-ms2_FT11.raw	Raw
	250304E_Vanessa_Dippon_SUB07258_TMT-ms2_FT12.raw	Raw

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