Mechanism of quinolone action: A drug-induced structural perturbation of the DNA precedes strand cleavage by topoisomerase IV Journal Article


Authors: Marians, K. J.; Hiasa, H.
Article Title: Mechanism of quinolone action: A drug-induced structural perturbation of the DNA precedes strand cleavage by topoisomerase IV
Abstract: Quinolones are potent broad spectrum antibacterial drugs that target the bacterial type II DNA topoisomerases. Their cytotoxicity derives from their ability to shift the cleavage-religation equilibrium required for topoisomerase action toward cleavage, thereby effectively trapping the enzyme on the DNA. It has been proposed that these drugs act by binding to the enzyme-DNA complex. Using catalytically inactive and quinolone-resistant mutant topoisomerase IV proteins, nitrocellulose filter DNA binding assays, and KMnO4 probing of drug-DNA and drug-DNA-enzyme complexes, we show:. (i) that norfloxacin binding to DNA induces a structural alteration, which probably corresponds to an unwinding of the helix, that is exacerbated by binding of the topoisomerase and by binding of the drug to the enzyme and (ii) that formation of this structural perturbation in the DNA precedes DNA cleavage by the topoisomerase in the ternary complex. We conclude that cleavage of the DNA and the resultant opening of the DNA gate during topoisomerization requires the induction of strain in the DNA that is bound to the enzyme. We suggest that quinolones may act to accelerate the rate of DNA cleavage by stimulating acquisition of this structural perturbation in the ternary complex.
Keywords: cytotoxicity; dna strand breakage; dna; drug mechanism; enzyme inhibitors; binding site; mutagenesis, site-directed; binding sites; nucleic acid conformation; dna binding; dna topoisomerases, type ii; dna topoisomerase iv; dna topoisomerase; antibacterial activity; dna, superhelical; thymine; norfloxacin; quinolone derivative; priority journal; article; drug dna interaction; potassium permanganate
Journal Title: Journal of Biological Chemistry
Volume: 272
Issue: 14
ISSN: 0021-9258
Publisher: American Society for Biochemistry and Molecular Biology  
Date Published: 1997-04-04
Start Page: 9401
End Page: 9409
Language: English
DOI: 10.1074/jbc.272.14.9401
PUBMED: 9083078
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 17 March 2017 -- Source: Scopus
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  1. Kenneth Marians
    138 Marians
  2. Hiroshi   Hiasa
    21 Hiasa