Conversation 11: No. 2

category image Volume: Conversation 11
Issue Number 2
May 2000
ISBN 0-940030-81-0

Stabilization of Double Stranded Homologous Poly(dA)·Poly(dT) by Taxol

The nucleic acid activity of taxol and paclitaxel was investigated with synthetic and natural oligo- and polynucleotides. The polynucleotides poly(dA)·poly(dT), poly(dG)·poly(dC), poly[d(A-T)]·poly[d(A-T)], poly[d(G-C)]·poly[d(G-C)] and calf thymus DNA were used. The oligonucleotides are 24-mers with d(purine)24 ·d(pyrimidine)24 strands, as well as d[(purine)x-(pyrimidine)x]·d[(purine)x-(pyrimidine)x] sequences. The study was performed with spectroscopic and calorimetric methods in dilute and condensed DNA-solutions.

In a recent study, taxol and paclitaxel showed molecular recognition of AT nucleotides with a high affinity to homologous (dA)·(dT) sequences; no interaction with GC nucleotides could be observed. An astonishing stabilization of the DNA duplex up to DTm = 25°C was measured by thermal denaturation with poly(dA)·poly(dT)/paclitaxel complexes. Circular dichroism signals of DNA (24-mer) containing homologous (dA)·(dT) tracts increased with increasing amount of the drug; for the other oligo- and polynucleotides no change in the spectra could be found. Contrary to this findings, circular dichroism (CD) spectra of poly(dA)·poly(dT)/paclitaxel complexes displayed reduced intensities of the signals at increasing drug concentrations.

These findings in dilute solutions were complemented by differential scanning calorimetric investigations in condensed states (only calf thymus DNA tested). Increasing enthalpies by increasing amount of the drug point to a stabilization.

Simple phosphate backbone interaction in the narrow groove of (dA)·(dT) tracts could be a sufficient explanation for all the results. Hydrophilic side groups of the drug interact with the phosphate and clip the strands together, while the hydrophobic parts of the molecule may disturb the polynucleobase formation.

Gerlinde Bischoff1
Ulrich Gromann1
Sabine Lindau1
Eckhard Birch-Hirschfeld 2
Robert Bischoff3
Christian Bohley1
Walter-Vesély Meister1
and Siegfried Hoffmann1

1Martin Luther University Halle-Wittenberg
Institute of Biochemistry
Kurt-Mothes-Str. 3
D-06120 Halle (Saale), Germany
1Friedrich Schiller University
Institute of Virology
D-07745 Jena, Germany
3Sensobi Sensoren GmbH
Weinbergweg 22
D-06120 Halle (Saale), Germany


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