Shoji Takada
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Shoji Takada has a total of 1 co-authors. Here are the top co-authors by number of shared publications:
- Peter G. Wolynes
Department of Physics Department of Chemistry and Biochemistry Center for Theoretical Biological Physics University of California San Diego 92093 La Jolla CA
4 shared publications
Latest Publications
- 8 December 1997
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 107 (22) , 9585-9598
Microscopic theory of critical folding nuclei and reconfiguration activation barriers in folding proteins
An explicit droplet calculation is developed to address two aspects of the folding kinetics of large proteins: the thermodynamic folding barrier and the reconfiguration rate. First, a nonspecific folding nucleus is described as the instanton or dropletsolution of a free energy functional derived for a minimally frustrated polymer Hamiltonian of the Gō type. Second, a theory for the barriers for transitions between trapped misfolded states is developed using a replica approach extended to inhomogeneous cases near the glass transition temperature of a random heteropolymer. Replica instantons are computed and their shape described. These two factors are then combined to give a microscopic theory of the folding time.
- 8 December 1997
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 107 (22) , 9585-9598
Microscopic theory of critical folding nuclei and reconfiguration activation barriers in folding proteins
An explicit droplet calculation is developed to address two aspects of the folding kinetics of large proteins: the thermodynamic folding barrier and the reconfiguration rate. First, a nonspecific folding nucleus is described as the instanton or dropletsolution of a free energy functional derived for a minimally frustrated polymer Hamiltonian of the Gō type. Second, a theory for the barriers for transitions between trapped misfolded states is developed using a replica approach extended to inhomogeneous cases near the glass transition temperature of a random heteropolymer. Replica instantons are computed and their shape described. These two factors are then combined to give a microscopic theory of the folding time.
- 1 April 1997
- Published by American Physical Society (APS) in Physical Review E
- Vol. 55 (4) , 4562-4577
Statics, metastable states, and barriers in protein folding: A replica variational approach
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.- 1 April 1997
- Published by American Physical Society (APS) in Physical Review E
- Vol. 55 (4) , 4562-4577
Statics, metastable states, and barriers in protein folding: A replica variational approach
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.- Open Access
- 1 January 1997
- Published by Oxford University Press (OUP) in Progress of Theoretical Physics Supplement
- Vol. 126, 49-52
Glassy Dynamics of Random Heteropolymers
The dynamics of random heteropolymers and their rugged free energy landscape are studied using a replica approach. Metastable states, barriers between lowest minima, entropic droplets are calculated between the static and dynamic glass transition temperatures.
- 1 January 1997
- Published by Oxford University Press (OUP) in Progress of Theoretical Physics Supplement
- Vol. 126, 49-52
Open AccessGlassy Dynamics of Random Heteropolymers
The dynamics of random heteropolymers and their rugged free energy landscape are studied using a replica approach. Metastable states, barriers between lowest minima, entropic droplets are calculated between the static and dynamic glass transition temperatures.
- 1 January 1997
- Published by Oxford University Press (OUP) in Progress of Theoretical Physics Supplement
- Vol. 126, 49-52
Glassy Dynamics of Random Heteropolymers
- 1 January 1997
- Published by Oxford University Press (OUP) in Progress of Theoretical Physics Supplement
- Vol. 126, 49-52
Glassy Dynamics of Random Heteropolymers