| Literature DB >> 30681906 |
Raimo Franke1, Bettina Hinkelmann1, Verena Fetz1, Theresia Stradal2, Florenz Sasse1, Frank Klawonn3,4, Mark Brönstrup1,5.
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.Entities:
Keywords: actinomycin D; impedance spectroscopy; mode of action; natural products; target identification
Mesh:
Year: 2019 PMID: 30681906 DOI: 10.1177/2472555218819459
Source DB: PubMed Journal: SLAS Discov ISSN: 2472-5552 Impact factor: 3.341