| Literature DB >> 34137598 |
Julie M Garlick1,2, Steven M Sturlis1,2, Paul A Bruno1,2, Joel A Yates3, Amanda L Peiffer1,4, Yejun Liu1,4, Laura Goo3, LiWei Bao3, Samantha N De Salle1,4, Giselle Tamayo-Castillo5, Charles L Brooks2,4,6, Sofia D Merajver3, Anna K Mapp1,2,4.
Abstract
Inhibitors of transcriptional protein-protein interactions (PPIs) have high value both as tools and for therapeutic applications. The PPI network mediated by the transcriptional coactivator Med25, for example, regulates stress-response and motility pathways, and dysregulation of the PPI networks contributes to oncogenesis and metastasis. The canonical transcription factor binding sites within Med25 are large (∼900 Å2) and have little topology, and thus, they do not present an array of attractive small-molecule binding sites for inhibitor discovery. Here we demonstrate that the depsidone natural product norstictic acid functions through an alternative binding site to block Med25-transcriptional activator PPIs in vitro and in cell culture. Norstictic acid targets a binding site comprising a highly dynamic loop flanking one canonical binding surface, and in doing so, it both orthosterically and allosterically alters Med25-driven transcription in a patient-derived model of triple-negative breast cancer. These results highlight the potential of Med25 as a therapeutic target as well as the inhibitor discovery opportunities presented by structurally dynamic loops within otherwise challenging proteins.Entities:
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Year: 2021 PMID: 34137598 PMCID: PMC8717358 DOI: 10.1021/jacs.1c03258
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419