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xCELLanalyzer: A Framework for the Analysis of Cellular Impedance Measurements for Mode of Action Discovery

  • Raimo Franke*
  • , Bettina Hinkelmann
  • , Verena Fetz
  • , Theresia Stradal
  • , Florenz Sasse
  • , Frank Klawonn
  • , Mark Brönstrup*
  • *Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer review

Abstract

Mode of action (MoA) identification of bioactive compounds is very often a challenging and time-consuming task. We used a label-free kinetic profiling method based on an impedance readout to monitor the time-dependent cellular response profiles for the interaction of bioactive natural products and other small molecules with mammalian cells. Such approaches have been rarely used so far due to the lack of data mining tools to properly capture the characteristics of the impedance curves. We developed a data analysis pipeline for the xCELLigence Real-Time Cell Analysis detection platform to process the data, assess and score their reproducibility, and provide rank-based MoA predictions for a reference set of 60 bioactive compounds. The method can reveal additional, previously unknown targets, as exemplified by the identification of tubulin-destabilizing activities of the RNA synthesis inhibitor actinomycin D and the effects on DNA replication of vioprolide A. The data analysis pipeline is based on the statistical programming language R and is available to the scientific community through a GitHub repository.

Original languageEnglish
Pages (from-to)213-223
Number of pages11
JournalSLAS Discovery
Volume24
Issue number3
E-pub ahead of print25 Jan 2019
DOIs
Publication statusPublished - Mar 2019

Keywords

  • actinomycin D
  • impedance spectroscopy
  • mode of action
  • natural products
  • target identification

ASJC Scopus subject areas

  • Biotechnology
  • Analytical Chemistry
  • Biochemistry
  • Molecular Medicine

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