Binding of two novel bisdaunorubicins to DNA studied by NMR spectroscopy

Howard Robinson, Waldemar Priebe, Jonathan B. Chaires, Andrew H.J. Wang

Research output: Contribution to journalArticlepeer-review

74 Citations (Scopus)


In the search for new generations of anthracycline drugs, lower cytotoxic side effects and higher activity against resistant cancer cells are two major goals. A new class of bis-intercalating anthracycline drugs has been designed, synthesized, and shown to have promising activity against multidrug-resistant cells. Two daunorubicins symmetrically linked together via a p-xylenyl group, either at their N3' (compound WP631) or N4' sites (compound WP652), exhibit extraordinary DNA binding affinities. We have used high-resolution NMR studies to understand the DNA binding mode of these two new bis-daunorubicin anticancer compounds. The structures of the WP631- d(ACGTACGT)2 and the WP652-d(TGTACA)2 complexes have been determined by NOE-restrained refinement. WP631 binds strongly to the 5'-CG(A/T)(A/T)CG hexanucleotide sequence, with the aglycons intercalated between the two CpG sites at both ends of the hexanucleotide sequence. The overall conformation of the WP631-d(CGTACG)2 part is remarkably similar to the crystal structure of the 2:1 complex of daunorubicin and d(CGTACG)2, as predicted previously [Gao, Y.-G., and Wang, A. H. J. (1996) J. Biomol. Struct. Dyn. 13, 103-117]. In contrast, the related bis-intercalator WP652 prefers the 5'-PyGTPu tetranucleotide sequence, with the aglycons intercalated between the PypG and TpPu sites. The binding of WP652 to DNA results in a severely distorted B- DNA duplex with the p-xylenyl tether moiety significantly protruded away from the bottom of the minor groove. While WP652 in some ways behaves similarly to other anticancer bis-intercalating antibiotics (e.g., triostine A and echinomycin), the detailed interactions between those two classes of bis- intercalators are quite different.

Original languageEnglish
Pages (from-to)8663-8670
Number of pages8
Issue number29
Publication statusPublished - Jul 22 1997
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry


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