## Abstract The broadening of a helix–coil transition due to base pair heterogeneity is calculated on the basis of a cumulant perturbation expansion in the quasi‐grand ensemble. In this ensemble the fictitious, homogeneous chain, to which the perturbation is referred, automatically decreases its co
Helix–coil transition in heterogeneous chains. II. DNA model
✍ Scribed by B. K. Eichinger; M. Fixman
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1970
- Tongue
- English
- Weight
- 843 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
Melting curves are calculated for infinitely long DNA‐like random copolymers composed of AT and GC pairs of nucleotides. The entropy of random coil rings formed on melting is explicitly included through use of the Jacobson‐Stockmayer ring‐weighting factors. Transition curves are calculated for values of the cooperativity parameter σ in the range 10^−2^ ⩽ σ ⩽ 10^−4^. Ninety percent of the melting occurs in ca. 0.2°C for σ ⩽ 10^−3^ regardless of the mole fraction of GC. We conclude that observed breadths of thermal denaturation curves for native DNAs result from a superposition of essentially all‐or‐none melting of various regions of the molecule. It is argued that refined approximations to the ring‐weighting factors are probably not important when compared with the effects produced by long‐range base sequence correlations which are known to occur in native DNA.
📜 SIMILAR VOLUMES
## Abstract An explicit analytical theory of DNA melting is constructed. It accounts for the loop entropy and the elasticity of DNA strands. Explicit analytical formulas are presented for the melting curves of natural DNA and periodic polymers. The nature of the DNA helix–coil transition is investi
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