| Literature DB >> 32618075 |
Tabea Schneidewind1,2, Alexandra Brause1, Axel Pahl1, Annina Burhop1, Tom Mejuch1, Sonja Sievers1, Herbert Waldmann1,2, Slava Ziegler1.
Abstract
Unbiased morphological profiling of bioactivity, for example, in the cell painting assay (CPA), enables the identification of a small molecule's mode of action based on its similarity to the bioactivity of reference compounds, irrespective of the biological target or chemical similarity. This is particularly important for small molecules with nonprotein targets as these are rather difficult to identify with widely employed target-identification methods. We employed morphological profiling using the CPA to identify compounds that are biosimilar to the iron chelator deferoxamine. Structurally different compounds with different annotated cellular targets provoked a shared physiological response, thereby defining a cluster based on their morphological fingerprints. This cluster is based on a shared mode of action and not on a shared target, that is, cell-cycle modulation in the S or G2 phase. Hierarchical clustering of morphological fingerprints revealed subclusters that are based on the mechanism of action and could be used to predict target-related bioactivity.Entities:
Keywords: antiproliferative; cell cycle; iron chelators; mode of action; phenotypic profiling
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Year: 2020 PMID: 32618075 PMCID: PMC7754162 DOI: 10.1002/cbic.202000381
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164