Reactive rifampicin derivative able to damage transcription complex

Maxim Kozlov, Eugeny Nudler, Vadim Nikiforov, Arkady Mustaev

Research output: Contribution to journalArticle

2 Scopus citations

Abstract

Rifampicin (Rif) is powerful broad spectrum antibiotic that targets bacterial RNA polymerase (RNAP) by blocking the transcript exit channel. The performance of the drug can be further enhanced by tagging with active chemical groups that produce collateral damage. We explored this principle by tethering Rif to Fe2+-EDTA chelate. Modified drug retained high binding affinity to RNAP and caused localized cleavage of the enzyme and promoter DNA. Analysis of the degradation products revealed the cleavage of RNAP β subunit at the sites involved in the drug binding, while DNA was selectively seized in the vicinity of the transcription start site. The synthesized Rif derivative exemplifies "aggressive" types of drugs that can be especially useful for TB treatment by attacking the nongrowing dormant form of the mycobacterium, which is hardly susceptible to "passive" drugs.

Original languageEnglish (US)
Pages (from-to)443-447
Number of pages5
JournalBioconjugate Chemistry
Volume24
Issue number3
DOIs
StatePublished - Mar 20 2013

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All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Bioengineering
  • Biomedical Engineering
  • Pharmacology
  • Pharmaceutical Science
  • Organic Chemistry

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