Free Energy Landscape of Protein-like Chains with Discontinuous Potentials
Hanif Bayat Movahed, Ramses van Zon, Jeremy Schofield

TL;DR
This study explores the free energy landscape of simplified protein models with discontinuous potentials, revealing funnel-like structures in short chains and multiple minima in longer chains, using advanced sampling methods.
Contribution
It introduces a novel analysis of protein-like chains with discontinuous potentials, demonstrating how chain length affects the free energy landscape and folding behavior.
Findings
Short chains exhibit funnel-like free energy landscapes at low temperatures.
Longer chains have multiple minima with degenerate lowest energy states.
Probability of most common configuration remains below one for longer chains.
Abstract
In this article the configurational space of two simple protein models consisting of polymers composed of a periodic sequence of four different kinds of monomers is studied as a function of temperature. In the protein models, hydrogen bond interactions, electrostatic repulsion, and covalent bond vibrations are modeled by discontinuous step, shoulder and square-well potentials, respectively. The protein-like chains exhibit a secondary alpha helix structure in their folded states at low temperatures, and allow a natural definition of a configuration by considering which beads are bonded. Free energies and entropies of configurations are computed using the parallel tempering method in combination with hybrid Monte Carlo sampling of the canonical ensemble of the discontinuous potential system. The probability of observing the most common configuration is used to analyze the nature of the…
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Taxonomy
TopicsProtein Structure and Dynamics · Proteins in Food Systems · Material Dynamics and Properties
