We consider theoretical aspects of reactions that form base pairs in a double helix. The equilibrium constant for such reactions depends on the probability of finding the two bases in the correct orientation for pairing. This probability can be expressed in terms of the spatial and angular distribut
On the B to A conformation change of the double helix
β Scribed by James M. Eyster; E. W. Prohofsky
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1977
- Tongue
- English
- Weight
- 974 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0006-3525
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β¦ Synopsis
Abstract
We have investigated the B to A conformation change of DNA double helices by a new method βsoftβmode analysis.β We find theoretically that a mode does soften when the vibration normal modes are perturbed by increasing the electrostatic interaction between the unbalanced charges on atoms in the double helix. The same mode also softens for enhanced van der Waals interactions. The mode softening indicates the onset of conformation change. The enhancing of the electrostatic and van der Waals interaction mimic the effect of decreasing the polar nature of the solvent or water of hydration associated with the B conformation DNA. We discuss qualitatively the concept of soft modes and their relation to conformation change as well as their applicability to macromolecules. We discuss previous work in which the normal vibrational modes have been calculated. We also discuss the displacement which comes from the soft mode and show that it correlates very well with that expected for the B to A conformation charge.
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