Affordable Access

deepdyve-link
Publisher Website

Regulating the ARNT/TACC3 axis: multiple approaches to manipulating protein/protein interactions with small molecules.

Authors
  • Guo, Yirui1
  • Partch, Carrie L
  • Key, Jason
  • Card, Paul B
  • Pashkov, Victor
  • Patel, Anjana
  • Bruick, Richard K
  • Wurdak, Heiko
  • Gardner, Kevin H
  • 1 Departments of Biophysics, UT Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-8816, USA.
Type
Published Article
Journal
ACS Chemical Biology
Publisher
American Chemical Society
Publication Date
Mar 15, 2013
Volume
8
Issue
3
Pages
626–635
Identifiers
DOI: 10.1021/cb300604u
PMID: 23240775
Source
Medline
Language
English
License
Unknown

Abstract

For several well-documented reasons, it has been challenging to develop artificial small molecule inhibitors of protein/protein complexes. Such reagents are of particular interest for transcription factor complexes given links between their misregulation and disease. Here we report parallel approaches to identify regulators of a hypoxia signaling transcription factor complex, involving the ARNT subunit of the HIF (Hypoxia Inducible Factor) activator and the TACC3 (Transforming Acidic Coiled Coil Containing Protein 3) coactivator. In one route, we used in vitro NMR and biochemical screening to identify small molecules that selectively bind within the ARNT PAS (Per-ARNT-Sim) domain that recruits TACC3, identifying KG-548 as an ARNT/TACC3 disruptor. A parallel, cell-based screening approach previously implicated the small molecule KHS101 as an inhibitor of TACC3 signaling. Here, we show that KHS101 works indirectly on HIF complex formation by destabilizing both TACC3 and the HIF component HIF-1α. Overall, our data identify small molecule regulators for this important complex and highlight the utility of pursuing parallel strategies to develop protein/protein inhibitors.

Report this publication

Statistics

Seen <100 times