## Abstract The helix–coil transition in poly(γ‐benzyl L‐glutamate‐__co__‐γ‐methyl L‐glutamate) copolypeptides was studied experimentally in nonaqueous solvents and the results compared with theory. It is found that the transition can be described by the same theory as for the homopolypeptides, but
Helix-coiled transition in heteropolymers. I. Ground-state energy
✍ Scribed by A. Vilenkin
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1977
- Tongue
- English
- Weight
- 722 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
A new technique is presented for treating the ground state of an heteropolymer with a random sequence of components. An exact system of equations is found for determining the ground state energy E which is equal to the polymer free energy f in the lowest-order approximation in TIV (Vl2 is the large "surface" energy arising a t the boundaries between coiled and "helical" sections: V >> T, Uk; U1 and -U2 are the free energies of the components counted from the corresponding coiled state energies). These equations are essentially simplified a t certain fixed values of the ratio U1/U2. For integer values of U2IU1 and U1IU2 a solution is obtained with an accuracy exp(-VIUk). The ground-state energy as a function of U1 and 112 is shown to be highly irregular: its derivatives have jumps a t an infinite number of points. These jumps provide a fine structure of the melting curves. A smoothed over the jumps function E' is found by way of analytic continuation from the integer values of UlIU2 and U2/Ul. The accuracy of the approximation f = E is estimated and the correctional term of order TIV is determined. *This work was done in partial fulfillment of the Ph.D. degree requirements of the Department of Physics, SUNY at Buffalo.
📜 SIMILAR VOLUMES
The helix-coil transit.iotis for poly(L-glutamic acid) (PGA) in 0.2M NaCl and ill its mixture with dioxane were studied by the methods of spectropolarimetry, viscometry, and potentiometric titration at different temperatures from 8 to 50°C. The enthalpy and entropy differences between the helical an
The Lifson-Roig and Zimm-Bragg theories of t,he helix-coil transition ill polypeptides are generalized to include both right-and left-handed a-helical states. The partition functions for these more general theories are formulated in terms of the parameters u, V R , V L , W R , and W L for t,he gener
We use heat capacity data of Taylor et al. to calculate the enthalpy distribution of a model peptide using the moments/maximum-entropy method. The peptide was designed with small covalent loops at both ends of the molecule to nucleate ␣-helix thus giving a system that would be expected to show a hel
## Abstract The enthalpies of the helix‐coil transitions of the ordered polynucleotide systems of poly(inosinic acid)–poly(cytidylic acid) [poly(I + C)], (helical duplex), and of poly (inosinic acid) [poly(I + I + I)], (proposed secondary structure: a triple‐stranded helical complex), were determin