Assessing sensitivity to antibacterial topoisomerase II inhibitors.

Sonia K. Morgan-Linnell, Hiroshi Hiasa, Lynn Zechiedrich, John L. Nitiss

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Both prokaryotes and eukaryotes have two major classes of topoisomerases that make transient single- or double-strand cuts in DNA. While these enzymes play critical roles in cellular processes, they are also important targets of therapeutic agents. This unit describes assays to use in characterizing topoisomerase II-targeting agents in vitro and in bacterial cells. It provides protocols for characterizing the action of small molecules against bacterial type II topoisomerases in vitro and the in vivo effects of putative topoisomerase II-targeting antibiotics, as well as for measuring trapped enzyme/DNA covalent complexes, the major cytotoxic lesion induced by fluoroquinolones.

Original languageEnglish (US)
Pages (from-to)Unit3.13
JournalCurrent protocols in pharmacology / editorial board, S.J. Enna (editor-in-chief) ... [et al.]
VolumeChapter 3
DOIs
StatePublished - Dec 2007

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