Arylstibonic acids: Novel inhibitors and activators of human topoisomerase IB

Hyeongnam Kim, John H. Cardellina, Rhone Akee, James J. Champoux, James T. Stivers

Research output: Contribution to journalArticlepeer-review

Abstract

Human topoisomerase IB (hTopo) forms a covalent phosphotyrosyl linkage with the DNA backbone, and controls genomic DNA topology by relaxing DNA supercoils during the processes of DNA replication, transcription, chromosome condensation and decondensation. The essential role of hTopo in these processes has made it a preeminent anticancer drug target. We have screened a small library of arylstibonic acids for their effects on plasmid supercoil relaxation catalyzed by hTopo. Despite the similar structures of the library compounds, some compounds were found to be effective competitive inhibitors, and others, nonessential activators. Some arylstibonic acids show selectivity in their action against hTopo and the related enzyme from poxvirus (vTopo). Structure-activity relationships and structural modeling suggest that competitive inhibition may result from positioning of the negatively charged stibonic acid and carboxylate groups of the inhibitors into DNA phosphate binding pockets on hTopo. The hTopo activators act by a surprising allosteric mechanism without interfering with DNA binding or binding of the widely used hTopo poison camptothecin. Arylstibonic acid competitive inhibitors may become useful small molecules for elucidating the cellular functions of hTopo.

Original languageEnglish (US)
Pages (from-to)190-197
Number of pages8
JournalBioorganic Chemistry
Volume36
Issue number4
DOIs
StatePublished - Aug 1 2008

Keywords

  • Arylstibonic acid inhibitors and activators
  • Topoisomerase IB

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Drug Discovery
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Arylstibonic acids: Novel inhibitors and activators of human topoisomerase IB'. Together they form a unique fingerprint.

Cite this