xCELLanalyzer: A Framework for the Analysis of Cellular Impedance Measurements for Mode of Action Discovery
Author(s) -
Franke Raimo,
Hinkelmann Bettina,
Fetz Verena,
Stradal Theresia,
Sasse Florenz,
Klawonn Frank,
Brönstrup Mark
Publication year - 2019
Publication title -
slas discovery
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.002
H-Index - 17
eISSN - 2472-5560
pISSN - 2472-5552
DOI - 10.1177/2472555218819459
Subject(s) - computer science , identification (biology) , pipeline (software) , mode of action , profiling (computer programming) , computational biology , data mining , chemistry , biology , botany , programming language , operating system , biochemistry
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.
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