Dependence of the hydration shell structure in the minor groove of the DNA double helix on the groove width as revealed by monte carlo simulation
✍ Scribed by A. V. Teplukhin; V. I. Poltev; V. P. Chuprina
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1991
- Tongue
- English
- Weight
- 669 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
The hydration shell of several conformations of the polynucleotides poly(dA) · poly(dT), poly (dA) · poly (dU), and poly (dA‐dl) · poly (dT‐dC) has been simulated using the Monte Carlo method (Metropolis sampling). Calculations have shown that the structure of the hydration shell of the minor groove greatly depends on its width. In conformations with a narrowed minor groove, the first layer of the hydration shell of this groove has only one molecule per nucleotide pair that forms H bonds with purine N3 of one pair and pyrimidine O2 of the next pair. The second layer of the hydration shell of such conformations contains molecules that form H bonds between two adjacent molecules of the first layer. The probability of formation of hydration spine is about 20% while the bridges of the first layer are formed with a probability of about 70%.
In the first layer of the minor groove of the B–DNA conformation with wide minor groove there are approximately two water molecules per base pair that form H bonds with purine N3 or pyrimidine O2 and with the sugar ring oxygen of the adjacent nucleotide. The probability of simultaneous H bonding of a water molecule with N3 (or O2) and O of sugar ring is about 30%.
The results of simulation suggest that hydration spine proposed for the narrowed minor groove of oligonucleotide crystals [H. R. Drew, and R. E. Dickerson (1981) Journal of Molecular Biology, Vol. 151, pp. 535–556] can be formed in fibers of poly (dA) · poly (dT), poly (dA) · poly (dU), and poly (dA‐dl) · poly (dT‐dC) as well as in DNA fragments of these sequences in solution. The role of the hydration shell of the minor groove of DNA double helix in stabilization of certain B‐family conformations is discussed.