On the Kinetic Behavior and Folding Properties of an Off-Lattice Heteropolymer Model
نویسنده
چکیده
The kinetic behavior of a three-dimensional off-lattice heteropolymer model is studied in terms of the time dependence of the average mean-square displacement between configurations. It is found that at short time-scales similar behavior is obtained even for sequences with very different thermodynamic properties. Furthermore, the degree of cooperativity in the folding process is examined by studying the residual number of degrees of freedom, obtained from an eigenvalue analysis of the correlation matrix, contributing to the structural fluctuations. In the compact state, a gradual decrease in this effective number of degrees of freedom take place as the temperature is lowered. This can be interpreted as an increasing asymmetry of the energy landscape.
منابع مشابه
Thermodynamic Studies of Macromolecular Models a Blocking Technique for Emulating Very Large Polyelectrolytes, Local Interactions and Protein Folding: a 3d Oo-lattice Approach, on the Kinetic Behavior and Folding Properties of an Oo-lattice Heteropolymer Model
LU TP 97-04 (submitted to Europhysics Letters).
متن کاملOn the Kinetic Behavior and Folding
The kinetic behavior of a three-dimensional oo-lattice heteropolymer model is studied in terms of the time dependence of the average mean-square displacement between conngura-tions. It is found that at short timescales similar behavior is obtained even for sequences with very diierent thermodynamic properties. Furthermore, the degree of cooperativity in the folding process is examined by studyi...
متن کاملFreezing and folding behavior in simple off-lattice heteropolymers.
We have performed parallel tempering Monte Carlo simulations using a simple continuum heteropolymer model for proteins. All 10 heteropolymer sequences which we have studied have shown first-order transitions at low temperature to ordered states dominated by single chain conformations. These results are in contrast with the theoretical predictions of the random energy model for heteropolymers, f...
متن کاملIdentification of characteristic protein folding channels in a coarse-grained hydrophobic-polar peptide model.
Folding channels and free-energy landscapes of hydrophobic-polar heteropolymers are discussed on the basis of a minimalistic off-lattice coarse-grained model. We investigate how rearrangements of hydrophobic and polar monomers in a heteropolymer sequence lead to completely different folding behaviors. Studying three exemplified sequences with the same content of hydrophobic and polar residues, ...
متن کاملTitle: Identification of Characteristic Protein Folding Channels in a Coarse- Grained Hydrophobic-polar Peptide Model
Folding channels and free-energy landscapes of hydrophobic-polar heteropolymers are discussed on the basis of a minimalistic off-lattice coarse-grained model. We investigate how rearrangements of hydrophobic and polar monomers in a heteropolymer sequence lead to completely different folding behaviors. Studying three exemplified sequences with the same content of hydrophobic and polar residues, ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 1997