Abstract
A comparative study on the intercalating binding of sanguinarine, chelerythrine, and nitidine with CT DNA, poly(dG-dC)·poly(dG-dC), poly(dA-dT)·poly(dA-dT), and seven sequence-designed double-stranded oligodeoxynucleotides has been performed using fluorometric and spectrophotometric techniques, aiming at providing insights into their sequence selectivity for DNA-binding. The results show that both sanguinarine and nitidine bind preferentially to DNA containing alternating GC base pairs [d(TGCGCA)2], while chelerythrine exhibits quite distinct sequence selectivity from sanguinarine, which shows a high specificity for DNA containing contiguous GC base pairs [5′-TGGGGA-3′/3′-ACCCCT-5′]. © 2006 Elsevier Ltd. All rights reserved.
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CITATION STYLE
Bai, L. P., Zhao, Z. Z., Cai, Z., & Jiang, Z. H. (2006). DNA-binding affinities and sequence selectivity of quaternary benzophenanthridine alkaloids sanguinarine, chelerythrine, and nitidine. Bioorganic and Medicinal Chemistry, 14(16), 5439–5445. https://doi.org/10.1016/j.bmc.2006.05.012
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