1. Academic Validation
  2. Medium-Throughput Detection of Hsp90/Cdc37 Protein-Protein Interaction Inhibitors Using a Split Renilla Luciferase-Based Assay

Medium-Throughput Detection of Hsp90/Cdc37 Protein-Protein Interaction Inhibitors Using a Split Renilla Luciferase-Based Assay

  • SLAS Discov. 2020 Feb;25(2):195-206. doi: 10.1177/2472555219884033.
Farid Ahmad Siddiqui 1 Hanna Parkkola 1 Ganesh Babu Manoharan 2 Daniel Abankwa 1 2
Affiliations

Affiliations

  • 1 Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
  • 2 Cancer Cell Biology and Drug Discovery Group, Life Sciences Research Unit, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
Abstract

The protein-folding chaperone HSP90 enables the maturation and stability of various oncogenic signaling proteins and is thus pursued as a Cancer drug target. Folding in particular of protein kinases is assisted by the co-chaperone Cdc37. Several inhibitors against the HSP90 ATP-binding site have been developed. However, they displayed significant toxicity in clinical trials. By contrast, the natural product conglobatin A has an exceptionally low toxicity in mice. It targets the protein-protein interface (PPI) of HSP90 and Cdc37, suggesting that interface inhibitors have an interesting drug development potential. In order to identify inhibitors of the HSP90/Cdc37 PPI, we have established a mammalian cell lysate-based, medium-throughput amenable split Renilla luciferase assay. This assay employs N-terminal and C-terminal fragments of Renilla luciferase fused to full-length human HSP90 and Cdc37, respectively. We expect that our assay will allow for the identification of novel HSP90/Cdc37 interaction inhibitors. Such tool compounds will help to evaluate whether the toxicity profile of HSP90/Cdc37 PPI inhibitors is in general more favorable than that of ATP-competitive HSP90 inhibitors. Further development of such tool compounds may lead to new classes of HSP90 inhibitors with applications in Cancer and Other Diseases.

Keywords

Hsp90/Cdc37 interaction inhibitors; assay development; drug discovery; protein–protein interface inhibitors; split Renilla luciferase.

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