Rezaei Adariani Soheila, Agne Daya, Koska Sandra, Burhop Annina, Seitz Carina, Warmers Jens, Janning Petra, Metz Malte, Pahl Axel, Sievers Sonja, Waldmann Herbert, Ziegler Slava
Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Strasse 11, 44227 Dortmund, Germany.
Faculty of Chemistry and Chemical Biology, Technical University Dortmund, Otto-Hahn-Strasse 6, 44227 Dortmund, Germany.
J Med Chem. 2024 Aug 8;67(15):13252-13270. doi: 10.1021/acs.jmedchem.4c01183. Epub 2024 Jul 17.
Mitochondria are cellular powerhouses and are crucial for cell function. However, they are vulnerable to internal and external perturbagens that may impair mitochondrial function and eventually lead to cell death. In particular, small molecules may impact mitochondrial function, and therefore, their influence on mitochondrial homeostasis is at best assessed early on in the characterization of biologically active small molecules and drug discovery. We demonstrate that unbiased morphological profiling by means of the cell painting assay (CPA) can detect mitochondrial stress coupled with the induction of an integrated stress response. This activity is common for compounds addressing different targets, is not shared by direct inhibitors of the electron transport chain, and enables prediction of mitochondrial stress induction for small molecules that are profiled using CPA.
线粒体是细胞的动力源,对细胞功能至关重要。然而,它们易受内部和外部干扰因素的影响,这些因素可能损害线粒体功能并最终导致细胞死亡。特别是小分子可能会影响线粒体功能,因此,在生物活性小分子的表征和药物发现过程中,最好尽早评估它们对线粒体稳态的影响。我们证明,通过细胞绘画分析(CPA)进行无偏形态学分析可以检测到与综合应激反应诱导相关的线粒体应激。这种活性在针对不同靶点的化合物中很常见,电子传递链的直接抑制剂并不具备,并且能够预测使用CPA分析的小分子的线粒体应激诱导情况。