## Synopsis A theory of equilibrium denaturation of proteins is suggested. According to this theory, a cornerstone of protein denaturation is disruption of tight packing of side chains in protein core. Investigation of this disruption is the object of this paper. It is shown that this disruption i
Theory of cooperative transitions in protein molecules. II. Phase diagram for a protein molecule in solution
โ Scribed by Alexey V. Finkelstein; Evgeny I. Shakhnovich
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1989
- Tongue
- English
- Weight
- 707 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0006-3525
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โฆ Synopsis
The thermodynamically stable states of denatured protein in solution are investigated. These states are distinguished from the native state by the absence of tight packing of side chains while the compactness of denatured protein may vary within a wide region. The following regimes are outlined:
- the "wet" molten globule, i.e., the compact state with pores occupied by solvent; 2. the swollen globule ("wet," of course); and 3. the coil.
The "dry" molten globule, when solvent does not penetrate inside the protein, is excluded for all experimental conditions. All the transitions within the denatured globule state are gradual while the denatured globule-coil phase transition is a second order one. The conditions of protein denaturation as well as conditions of transitions and crossovers within the denatured state are outlined.
๐ SIMILAR VOLUMES
## Abstract A mathematical model is developed adequately describing an unfolded polypeptide chain without longโrange interactions in which fluctuating hydrogenโbonded ฮฑโhelices, ฮฒโbends, fragments of helices 3~10~, and other local structures are formed. The obtained model is a modification of a one