A Ruthenium(II) Polypyridyl Complex Disrupts Actin Cytoskeleton Assembly and Blocks Cytokinesis.
Martin R GillPaul J JarmanVanessa HearndenSimon D FairbanksMarcella BassettoHannes MaibJohn PalmerKathryn R AyscoughJames A ThomasCarl SmythePublished in: Angewandte Chemie (Weinheim an der Bergstrasse, Germany) (2022)
The dinuclear Ru II complex [(Ru(phen) 2 ) 2 (tpphz)] 4+ (phen=1,10-phenanthroline, tpphz=tetrapyridophenazine) "RuRuPhen" blocks the transformation of G-actin monomers to F-actin filaments with no disassembly of pre-formed F-actin. Molecular docking studies indicate multiple RuRuPhen molecules bind to the surface of G-actin but not the binding pockets of established actin polymerisation inhibitors. In cells, addition of RuRuPhen causes rapid disruption to actin stress fibre organisation, compromising actomyosin contractility and cell motility; due to this effect RuRuPhen interferes with late-stage cytokinesis. Immunofluorescent microscopy reveals that RuRuPhen causes cytokinetic abscission failure by interfering with endosomal sorting complexes required for transport (ESCRT) complex recruitment.