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Fragment-Based Identification of Ligands for Bromodomain-Containing Factor 3 of Trypanosoma cruzi.

Corentine M C LaurinJoseph P BluckAnthony K C ChanMichelle KellerAndrew BoczekAmy R ScorahK F Larissa SeeLaura E JenningsDavid S HewingsFern WoodhouseJessica K ReynoldsMatthias SchiedelPhilip G HumphreysPhilip Charles BigginStuart J Conway
Published in: ACS infectious diseases (2020)
The Trypanosoma cruzi (T. cruzi) parasite is the cause of Chagas disease, a neglected disease endemic in South America. The life cycle of the T. cruzi parasite is complex and includes transitions between distinct life stages. This change in phenotype (without a change in genotype) could be controlled by epigenetic regulation, and might involve the bromodomain-containing factors 1-5 (TcBDF1-5). However, little is known about the function of the TcBDF1-5. Here we describe a fragment-based approach to identify ligands for T. cruzi bromodomain-containing factor 3 (TcBDF3). We expressed a soluble construct of TcBDF3 in E. coli, and used this to develop a range of biophysical assays for this protein. Fragment screening identified 12 compounds that bind to the TcBDF3 bromodomain. On the basis of this screen, we developed functional ligands containing a fluorescence or 19F reporter group, and a photo-crosslinking probe for TcBDF3. These tool compounds will be invaluable in future studies on the function of TcBDF3 and will provide insight into the biology of T. cruzi.
Keyphrases
  • trypanosoma cruzi
  • life cycle
  • high throughput
  • escherichia coli
  • crispr cas
  • current status
  • protein protein
  • quantum dots