Nucleic Acids Research, Vol 26, Issue 17 3949-3954, Copyright © 1998 by Oxford University Press
A Ferdous, H Watanabe, T Akaike and A Maruyama
Triplex DNA formation involving unmodified triplex-forming oligonucleotides
(TFOs) is very unstable under physiological conditions. Here, we report a
novel strategy to stabilize both purine and pyrimidine motif triplex DNA
within the rat alpha1 (I) collagen gene promoter under physiologically
relevant conditions by a poly(L- lysine)- graft -dextran copolymer. Using
an in vitro electrophoretic mobility shift assay, we show that the
copolymer almost completely abrogates the inhibitory effects of
physiological concentrations of monovalent cations, particularly potassium
ion (K+), on purine motif triplex formation involving very low
concentrations of an unmodified guanine-rich TFO. Of importance, pH
dependency in pyrimidine motif triplex formation involving an unmodified
cytosine-rich TFO is also significantly overcome by the copolymer. Finally,
the triplex- stabilizing efficiency of the copolymer is remarkably higher
than that of other oligocations, like spermine and spermidine. We suggest
that the ability of the graft copolymer to stabilize triplex DNA under
physiologically relevant pH and salt concentrations will be a cue for
further progress in the antigene strategy.
ARTICLES
Poly(L-lysine)-graft-dextran copolymer: amazing effects on triplex stabilization under physiological pH and ionic conditions (in vitro)
Department of Biomolecular Engineering, Faculty of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259 Nagatsuta, Midori- ku, Yokohama 226-8501, Japan.
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