Literature DB >> 12110628

Cell studies of the DNA bis-intercalator Delta-Delta [mu-C4(cpdppz)(2)-(phen)(4)Ru(2)](4+): toxic effects and properties as a light emitting DNA probe in V79 Chinese hamster cells.

Björn Onfelt1, Lovisa Göstring, Per Lincoln, Bengt Nordén, Agneta Onfelt.   

Abstract

Coordination complexes of type [Ru(L)(3)](2+), where L is a nitrogen-containing aromatic bidentate ligand, can often be photolytically reduced, making them useful in studies of DNA- or protein-mediated electron transfer and in artifical photosynthesis model systems. Upon binding to DNA some Ru(L) complexes have been found to display strongly increased fluorescence compared with when free in solution, making those compounds interesting to test as DNA probes. Thus, they are becoming widely used in the chemistry community. Here, asynchronous cultures of V79 Chinese hamster cells were exposed to the DNA bis-intercalator Delta-Delta [mu-C4(cpdppz)(2)-(phen)(4)Ru(2)](4+) at 10(-10)-10(-4) M. The extraordinarily strong binding of the compound to DNA was the reason for testing its possible interference with DNA metabolism in intact mammalian cells. Exposure for 1 h to 10(-10)-10(-4) M did not significantly decrease DNA synthesis. Cells exposed to 10(-5) M for 27 h showed no staining of the nucleus, while DNA was stained in cells electroporated in the presence of the compound. However, the Ru dimer was probably taken up by pinocytosis, because numerous minute precipitates could be observed in the cytoplasm. Treatment for 24 h at concentrations of 10(-10)-10(-5) M did not inhibit growth, as indicated by cell density and mitotic activity. Neither did it affect chromosomal arrangements during mitosis. However, at 10(-4) M the density of cultures was reduced by approximately 45% and apoptotic cells were frequent, as opposed to mitoses. We also investigated the properties of the Ru dimer as a fluorescent DNA stain. The compound appears attractive as a red DNA stain when broad excitation in the visible range is desirable and extremely low background staining is essential. The low toxicity of the compound is a favourable trait in this context.

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Year:  2002        PMID: 12110628     DOI: 10.1093/mutage/17.4.317

Source DB:  PubMed          Journal:  Mutagenesis        ISSN: 0267-8357            Impact factor:   3.000


  6 in total

1.  Methods to explore cellular uptake of ruthenium complexes.

Authors:  Cindy A Puckett; Jacqueline K Barton
Journal:  J Am Chem Soc       Date:  2007-01-10       Impact factor: 15.419

2.  Effects of chirality on the intracellular localization of binuclear ruthenium(II) polypyridyl complexes.

Authors:  Frida R Svensson; Johanna Andersson; Helene L Åmand; Per Lincoln
Journal:  J Biol Inorg Chem       Date:  2012-02-05       Impact factor: 3.358

3.  Biophysical studies of a ruthenium(II) polypyridyl complex binding to DNA and RNA prove that nucleic acid structure has significant effects on binding behaviors.

Authors:  Hong Xu; Yi Liang; Peng Zhang; Fen Du; Bing-Rui Zhou; Jun Wu; Jian-Hong Liu; Zhi-Gang Liu; Liang-Nian Ji
Journal:  J Biol Inorg Chem       Date:  2005-09-23       Impact factor: 3.358

4.  A ruthenium(II) polypyridyl complex for direct imaging of DNA structure in living cells.

Authors:  Martin R Gill; Jorge Garcia-Lara; Simon J Foster; Carl Smythe; Giuseppe Battaglia; Jim A Thomas
Journal:  Nat Chem       Date:  2009-10-18       Impact factor: 24.427

Review 5.  The development of anticancer ruthenium(ii) complexes: from single molecule compounds to nanomaterials.

Authors:  Leli Zeng; Pranav Gupta; Yanglu Chen; Enju Wang; Liangnian Ji; Hui Chao; Zhe-Sheng Chen
Journal:  Chem Soc Rev       Date:  2017-10-02       Impact factor: 54.564

6.  A ruthenium dimer complex with a flexible linker slowly threads between DNA bases in two distinct steps.

Authors:  Meriem Bahira; Micah J McCauley; Ali A Almaqwashi; Per Lincoln; Fredrik Westerlund; Ioulia Rouzina; Mark C Williams
Journal:  Nucleic Acids Res       Date:  2015-09-13       Impact factor: 16.971

  6 in total

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