RASPELD to Perform High-End Screening in an Academic Environment toward the Development of Cancer Therapeutics

ChemMedChem. 2018 Oct 8;13(19):2065-2072. doi: 10.1002/cmdc.201800477. Epub 2018 Aug 23.

Abstract

The identification of compounds for dissecting biological functions and the development of novel drug molecules are central tasks that often require screening campaigns. However, the required architecture is cost- and time-intensive. Herein we describe the devices and technologies that comprise a Robotics-Assisted Screening Platform for Efficient Ligand Discovery (RASPELD), which we set up in an academic laboratory. RASPELD provides semi-automated high-end screening, and it can be maintained by graduate students. We demonstrate its successful application in biochemical and cellular screens for the identification and validation of bioactive chemical entities as candidate cancer-relevant inhibitors. Specifically, we examined the interaction between a transcription factor, Nrf2, and its key regulator, Keap1. We also examined drug-resistant mutants of the epidermal growth factor receptor (EGFR). Screening campaigns with more than 30 000 compounds were performed in a reasonable period of time. We identified the molecule RSL6586 as a starting point for hit optimization, which is currently ongoing.

Keywords: cancer; drug discovery; hit validation; initial screen; medicinal chemistry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Biological Assay
  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical / instrumentation
  • Drug Evaluation, Preclinical / methods*
  • Education, Graduate
  • ErbB Receptors / antagonists & inhibitors
  • ErbB Receptors / genetics
  • Humans
  • Kelch-Like ECH-Associated Protein 1 / metabolism
  • Ligands
  • Mutation
  • NF-E2-Related Factor 2 / metabolism
  • Protein Binding / drug effects
  • Protein Kinase Inhibitors / pharmacology
  • Robotics / instrumentation
  • Robotics / methods*
  • Small Molecule Libraries / pharmacology*

Substances

  • Antineoplastic Agents
  • KEAP1 protein, human
  • Kelch-Like ECH-Associated Protein 1
  • Ligands
  • NF-E2-Related Factor 2
  • NFE2L2 protein, human
  • Protein Kinase Inhibitors
  • Small Molecule Libraries
  • EGFR protein, human
  • ErbB Receptors