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Tight Binding of the Antitumor Drug Ditercalinium to Quadruplex DNA

2002; Wiley; Volume: 3; Issue: 12 Linguagem: Inglês

10.1002/1439-7633(20021202)3

1439-7633

Carolina Carrasco, Frédéric Rosu, Valérie Gabelica, Claude Houssier, Edwin De Pauw, Christiane Garbay‐Jaureguiberry, Bernárd P. Roques, W. David Wilson, Jonathan B. Chaires, Michael J. Waring, Christian Bailly,

RNA Interference and Gene Delivery

The structural selectivity of the DNA-binding antitumor drug ditercalinium was investigated by competition dialysis with a series of nineteen different DNA substrates. The 7H-pyridocarbazole dimer was found to bind to double-stranded DNA with a preference for GC-rich species but can in addition form stable complexes with triplex and quadruplex structures. The preferential interaction of the drug with four-stranded DNA structures was independently confirmed by electrospray mass spectrometry and a detailed analysis of the binding reaction was performed by surface plasmon resonance (SPR) spectroscopy. The BIAcore SPR study showed that the kinetic parameters for the interaction of ditercalinium with the human telomeric quadruplex sequence are comparable to those measured with a duplex sequence. Slow association and dissociation were observed with both the quadruplex and duplex structures. The newly discovered preferential binding of ditercalinium to the antiparallel quadruplex sequence d(AG3[T2AG3]3) provides new perspectives for the design of drugs that can bind to human telomeres.