Statics, metastable states, and barriers in protein folding: A replica variational approach
- 1 April 1997
- journal article
- research article
- Published by American Physical Society (APS) in Physical Review E
- Vol. 55 (4) , 4562-4577
- https://doi.org/10.1103/physreve.55.4562
Abstract
Protein folding is analyzed using a replica variational formalism to investigate some free energy landscape characteristics relevant for dynamics. A random contact interaction model that satisfies the minimum frustration principle is used to describe the coil-globule transition (characterized by ), glass transitions (by and ), and folding transition (by ). Trapping on the free energy landscape is characterized by two characteristic temperatures, one dynamic () and the other static [ (>)], which are similar to those found in mean field theories of the Potts glass. (i) Above , the free energy landscape is monotonous and the polymer is melted both dynamically and statically. (ii) Between and , the melted phase is still dominant thermodynamically, but frozen metastable states, exponentially large in number, appear. (iii) A few lowest minima become thermodynamically dominant below , where the polymer is totally frozen. In the temperature range between and , barriers between metastable states are shown to grow with decreasing temperature, suggesting super-Arrhenius behavior in a sufficiently large system. Due to evolutionary constraints on fast folding, the folding temperature is expected to be higher than , but may or may not be higher than . Diverse scenarios of the folding kinetics are discussed based on phase diagrams that take into account the dynamical transition, as well as the static ones.
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