1. Academic Validation
  2. A Lipopeptidomimetic of Transcriptional Activation Domains Selectively Disrupts Med25 Protein-Protein Interactions

A Lipopeptidomimetic of Transcriptional Activation Domains Selectively Disrupts Med25 Protein-Protein Interactions

  • Angew Chem Int Ed Engl. 2024 Mar 25:e202400781. doi: 10.1002/anie.202400781.
Olivia N Pattelli 1 Estefanía Martínez Valdivia 2 Matthew S Beyersdorf 2 Clint S Regan 3 Mónica Rivas 1 Katherine A Hebert 4 Sofia D Merajver 5 Tomasz Cierpicki 6 Anna K Mapp 7
Affiliations

Affiliations

  • 1 University of Michigan, Life Sciences Institute, UNITED STATES.
  • 2 University of Michigan, Program in Chemical Biology, UNITED STATES.
  • 3 University of Michigan, Life Sciences institute, UNITED STATES.
  • 4 University of Michigan, Chemistry, UNITED STATES.
  • 5 University of Michigan Michigan Medicine, Internal Medicine, UNITED STATES.
  • 6 University of Michigan Michigan Medicine, Pathology, UNITED STATES.
  • 7 University of Michigan, Life Sciences Institute, 210 Washtenaw Ave, 48109, Ann Arbor, UNITED STATES.
Abstract

Short amphipathic Peptides are capable of binding to transcriptional coactivators, often targeting the same binding surfaces as native transcriptional activation domains. However, they do so with modest affinity and generally poor selectivity, limiting their utility as synthetic modulators. Here we show that incorporation of a medium-chain, branched fatty acid to the N-terminus of one such heptameric lipopeptidomimetic (LPPM-8) increases the affinity for the coactivator Med25 >20-fold (Ki >100 μM to 4 μM), rendering it an effective inhibitor of Med25 protein-protein interactions (PPIs). The lipid structure, the peptide sequence, and the C-terminal functionalization of the lipopeptidomimetic each influence the structural propensity of LPPM-8 and its effectiveness as an inhibitor. LPPM-8 engages Med25 through interaction with the H2 face of its Activator Interaction Domain and in doing so stabilizes full-length protein in the cellular proteome. Further, genes regulated by Med25-activator PPIs are inhibited in a cell model of triple-negative breast Cancer. Thus, LPPM-8 is a useful tool for studying Med25 and Mediator complex biology and the results indicate that lipopeptidomimetics may be a robust source of inhibitors for activator-coactivator complexes.

Keywords

Coactivator; Lipopeptide; Med25; Protein-protein interaction inhibitor; Transcription Factor.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-158104
    Med25 PPI Inhibitor