Multicanonical study of coarse-grained off-lattice models for folding heteropolymers

Phys Rev E Stat Nonlin Soft Matter Phys. 2005 Mar;71(3 Pt 1):031906. doi: 10.1103/PhysRevE.71.031906. Epub 2005 Mar 17.

Abstract

We have performed multicanonical simulations of hydrophobic-hydrophilic heteropolymers with two simple effective, coarse-grained off-lattice models to study the influence of specific interactions in the models on conformational transitions of selected sequences with 20 monomers. Another aspect of the investigation was the comparison with the purely hydrophobic homopolymer and the study of general conformational properties induced by the "disorder" in the sequence of a heteropolymer. Furthermore, we applied an optimization algorithm to sequences with up to 55 monomers and compared the global-energy minimum found with lowest-energy states identified within the multicanonical simulation. This was used to find out how reliable the multicanonical method samples the free-energy landscape, in particular for low temperatures.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Computer Simulation
  • Dimerization
  • Models, Chemical*
  • Models, Molecular*
  • Multiprotein Complexes / chemistry*
  • Polymers / chemistry*
  • Protein Binding
  • Protein Conformation
  • Protein Folding
  • Proteins / chemistry*

Substances

  • Multiprotein Complexes
  • Polymers
  • Proteins