Free Energy Landscape of a Protein-Like Chain in a Fluid with Discontinuous Potentials
Hanif Bayat Movahed, Ramses van Zon, Jeremy Schofield

TL;DR
This study explores the free energy landscape of a protein-like chain in a fluid with discontinuous potentials, revealing how solvent interactions influence protein folding structures and transition temperatures.
Contribution
It introduces a model combining discontinuous molecular dynamics with explicit solvent effects, advancing understanding of solvent influence on protein folding landscapes.
Findings
Helical and collapsed structures dominate at low temperatures.
Solvent presence raises the temperature for helical structure dominance.
Phase transitions in solvent hinder low-temperature exploration of the landscape.
Abstract
The free energy landscape of a protein-like chain in a fluid was studied by combining discontinuous molecular dynamics and parallel tempering. The model protein is a repeating sequence of four different beads, with interactions mimicking those in real proteins. Neighbor distances and angles are restricted to physical ranges and one out of the four kinds of beads can form hydrogen bonds with each other, except if they are too close in the chain. In contrast to earlier studies of this model, an explicit square-well solvent is included. Beads that can form intra-chain hydrogen bonds, can also form (weaker) hydrogen bonds with solvent molecules, while other beads are insoluble. By categorizing the protein configurations according to their intra-chain bonds, one can distinguish unfolded, helical, and collapsed helical structures. Simulations for chains of 15, 20 and 25 beads show that at low…
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Taxonomy
TopicsProteins in Food Systems · Protein Structure and Dynamics · Material Dynamics and Properties
