Activity of Quinolone CP-115,955 Against Bacterial and Human Type II Topoisomerases Is Mediated by Different Interactions
Year: 2015
Type: article
Abstract: CP-115,955 is a quinolone with a 4-hydroxyphenyl at C7 that displays high activity against both bacterial and human type II topoisomerases. To determine the basis for quinolone cross-reactivity between bacterial and human enzymes, the activity of CP-115,955 and a series of related quinolones and quinazolinediones against Bacillus anthracis topoisomerase IV and human topoisomerase IIα was analyzed. Results indicate that the activity of CP-115,955 against the bacterial and human enzymes is mediated by different interactions. On the basis of the decreased activity of quinazolinediones against wild-type and resistant mutant topoisomerase IV and the low activity of quinolones against resistant mutant enzymes, it appears that the primary interaction of CP-115,955 with the bacterial system is mediated through the C3/C4 keto acid and the water-metal ion bridge. In contrast, the drug interacts with the human enzyme primarily through the C7 4-hydroxyphenyl ring and has no requirement for a substituent at C8 in order to attain high activity. Despite the fact that the human type II enzyme is unable to utilize the water-metal ion bridge, quinolones in the CP-115,955 series display higher activity against topoisomerase IIα in vitro and in cultured human cells than the corresponding quinazolinediones. Thus, quinolones may be a viable platform for the development of novel drugs with anticancer potential.
Source: Biochemistry
DOI: 10.1021/bi501073v
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Awards: Structure and Function of the B. anthracis Exosporium, G1852395141, G4041358501, Predoctoral Training Program in Biotechnology, Function and Biology of Eukaryotic DNA Topoisomerases, G6817323303, G705680629, Antibacterial Agents that Restrict the Emergence of Resistance, G8814259252, Biochemical and Chemical Training for Cancer Research
OpenAlex ID: W2037105242
