Evaluation of complexes of DNA duplexes and novel benzoxazoles or benzimidazoles by electrospray ionization mass spectrometry |
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Authors: | Leon?Oehlers,Carolyn?L.?Mazzitelli,Jennifer?S.?Brodbelt mailto:jbrodbelt@mail.utexas.edu" title=" jbrodbelt@mail.utexas.edu" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author,Mireya?Rodriguez,Sean?Kerwin |
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Affiliation: | Department of Chemistry and Biochemistry, The University of Texas at Austin, Austin, Texas 78712-0165, USA. |
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Abstract: |  Electrospray ionization mass spectrometry is used to compare the metal ion binding and metal-mediated DNA binding of benzoxazole (1, 2, 3, 4) and benzimidazole (5) compounds and to elucidate the putative binding modes and stoichiometries. The observed metal versus non-metal-mediated DNA binding, as well as the specificity of DNA binding, is correlated with the biological activities of the analogs. The ESI-MS spectra for the antibacterial benzoxazole and benzimidazole analogs 4 and 5 demonstrated non-specific and non-metal-mediated binding to DNA, with the appearance of DNA complexes containing multiple ligands. The anticancer analog 2 demonstrates a clear preference for metal-mediated DNA interactions, with an apparent selectivity for Ni2+ -mediated binding over the more physiologically relevant Mg2+ or Zn2+ cations. Complexation between DNA and the biologically inactive analog 1 was not observed, either in the absence or presence of metal cations. |
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