Journal
BIOPOLYMERS
Volume 73, Issue 5, Pages 542-555Publisher
WILEY
DOI: 10.1002/bip.10583
Keywords
cation-DNA interactions; spermine; spermidine; putrescine; polyelectrolytes
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Molecular dynamics (MD) computer simulations have been carried out on four systems that correspond to an infinite array, of parallel ordered B-DNA, mimicking the state in oriented DNA,fibers and also being relevant,for crystals of B-DNA oligonucteotides. The systems were all comprised of a periodical hexagonal cell with three identical DNA decanters, 15 water molecules per nucleotide, and counterions balancing the DNA charges. The sequence of the double helical DNA decamer was d(5'-ATGCAGTCAG)xd(5'-TGACTGCATC). The counterions were the two natural polyamines spermidine(3+) (Spd(3+)) and putrescine(2+) (Put(2+)), the synthetic polyamine diaminopropane(2+) (DAP(2+)), and the simple monovalent cation Na+. This work compares the specific structures of the polyamine- and affected by counterion interactions. It also describes sequence Na-DNA systems and how they are (if specific hydration and interaction of the cations with DNA. The local DNA structure is dependent on the nature of the counterion. Even the very similar polyamines, Put(2+) and DAP(2+), show clear differences in binding to DNA and in effect on hydration and local structure. Generally, the polyamines disorder the hydration of the DNA around their binding sites whereas Na+ being bound to DNA attracts and organizes water in its vicinity. Cation binding at the selected sites in the minor and in the major groove is compared for the different polyamines and Na+. We conclude that the synthetic polyamine (DAP(2+)) binds specffically to several structural and sequence-specific motifs on B-DNA, unlike the natural polyamines, Spd(3+) and Put(2+). This specificity of DAP(2+) compared to the more dynamic behavior of Spd(3+) and Put(2+) may explain why the latter polyamines are naturally occurring in cells. (C) 2004 Wiley Periodicals, Inc.
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