Observation of non-covalent interactions between beauvericin and oligonucleotides using electrospray ionization mass spectrometry

Rapid Commun Mass Spectrom. 1997;11(3):265-72. doi: 10.1002/(SICI)1097-0231(19970215)11:3<265::AID-RCM848>3.0.CO;2-2.

Abstract

Electrospray ionization mass spectrometry has been used to study the possible non-covalent interaction between oligonucleotides and beauvericin (B) mycotoxin. Beauvericin-oligonucleotide adduct formation was observed even at low mycotoxin concentration (25 pmol/microL). Adducts were found with different numbers of B ligands attached. The selectivity of binding of B ligands to two different oligonucleotides has been shown to be similar indicating that beauvericin does not have a strongly preferred base sequence or base site in the DNA. In a competitive complexation reaction, beauvericin forms specific adducts with oligonucleotide while another mycotoxin, nigeromicin, which causes apoptosis without fragmentation of DNA, does not.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemistry*
  • Anti-Bacterial Agents / isolation & purification
  • DNA Fragmentation / drug effects
  • DNA, Fungal / analysis
  • Depsipeptides*
  • Fermentation
  • Fusarium / metabolism
  • Mass Spectrometry
  • Oligonucleotides / chemistry*
  • Peptides*

Substances

  • Anti-Bacterial Agents
  • DNA, Fungal
  • Depsipeptides
  • Oligonucleotides
  • Peptides
  • beauvericin