Journal
CANADIAN JOURNAL OF CHEMISTRY
Volume 82, Issue 6, Pages 1112-1118Publisher
CANADIAN SCIENCE PUBLISHING
DOI: 10.1139/V04-061
Keywords
DNA; RNA; taxol; binding site; binding constant; conformation; helix stability; electrophoresis; FTIR spectroscopy
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Taxol (paclitaxel) is an anticancer drug that interacts with microtubule proteins in a manner that catalyzes their formation from tubulin and stabilizes the resulting structures. However, in the human lung tumor cell, the concentration of paclitaxel is highest in the nucleus. Therefore, it was of interest to examine the interaction of taxol with DNA and RNA in aqueous solution at physiological pH. Capillary electrophoresis and Fourier transform infrared (FTIR) difference spectroscopic methods were used to characterize the nature of drug-DNA and drug-RNA interactions and to determine the taxol binding site, the binding constant, the sequence selectivity, the helix stability, and the biopolymer secondary structure in the taxol-polynucleotide complexes in vitro. The FTIR spectroscopic studies were conducted with taxol/polynucleotide (phosphate) ratios of 1/80, 1/40, 1/20, 1/10, 1/4, and 1/2 with a final DNA(P) or RNA(P) concentration of 12.5 mmol/L, and capillary electrophoresis was performed after incubation of taxol with polynucleotides at ratios of 1/200 to 1/12 with a final polynucleotide concentration of 1.25 mmol/L. Taxol was shown to bind to DNA and RNA at G-C, A-T, or A-U bases and the backbone PO2 group. Two types of binding were observed for taxol-DNA with K-1 = 1.3 x 10(4) L mol(-1) and K-2 = 3.5 x 10(3) L mol(-1), whereas taxol-RNA complexes showed one type of binding with K = 1.3 x 10(4) L mol(-1). The taxol-polynucleotide complexation is associated with a partial helix stabilization and no major alterations of B-DNA or A-RNA structure.
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