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Issue 33, 2015
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Recognition of DNA/RNA bulges by antimicrobial and antitumor metallohelices

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Bulged structures have been identified in nucleic acids and have been shown to be linked to biomolecular processes involved in numerous diseases. Thus, chemical agents with affinity for bulged nucleic acids are of general biological significance. Herein, the mechanism of specific recognition and stabilization of bulged DNA and RNA by helical bimetallic species was established through detailed molecular biophysics and biochemistry assays. These agents, known as ‘flexicates’, are potential mimetics of α-helical peptides in cancer treatment, exhibiting antimicrobial and antitumor effects. The flexicates have positive impacts on the thermal stability of DNA duplexes containing bulges, which means that the flexicates interact with the duplexes containing bulges, and that these interactions stabilize the secondary structures of these duplexes. Notably, the stabilising effect of the flexicates increases with the size of the bulge, the maximal stabilization is observed for the duplexes containing a bulge composed of at least three bases. The flexicates bind most preferentially to the bulges composed of pyrimidines flanked on both sides also by pyrimidines. It is suggested that it is so because these bulges exhibit greatest conformational variability in comparison with other combinations of bases in the bulge loop and bases flanking the bulge. Finally, the results indicate that there is only one dominant binding site for the flexicates on the DNA and RNA bulges and that the flexicates bind directly to the bulge or in its close proximity. It is also shown that the flexicates effectively bind to RNA duplexes containing the bulged region of HIV-1 TAR RNA.

Graphical abstract: Recognition of DNA/RNA bulges by antimicrobial and antitumor metallohelices

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Supplementary files

Article information

28 May 2015
10 Jul 2015
First published
14 Jul 2015

Dalton Trans., 2015,44, 14656-14665
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Author version available

Recognition of DNA/RNA bulges by antimicrobial and antitumor metallohelices

J. Malina, P. Scott and V. Brabec, Dalton Trans., 2015, 44, 14656
DOI: 10.1039/C5DT02018B

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