A Note on the Effects of Linear Topology Preservation in Monte Carlo Simulations of Knotted Proteins

  1. Especial, João N. C.
  2. Rey, Antonio
  3. Faísca, Patrícia F. N.
Aldizkaria:
International Journal of Molecular Sciences

ISSN: 1422-0067

Argitalpen urtea: 2022

Alea: 23

Zenbakia: 22

Orrialdeak: 13871

Mota: Artikulua

DOI: 10.3390/IJMS232213871 GOOGLE SCHOLAR lock_openSarbide irekia editor

Beste argitalpen batzuk: International Journal of Molecular Sciences

Laburpena

Monte Carlo simulations are a powerful technique and are widely used in different fields. When applied to complex molecular systems with long chains, such as those in synthetic polymers and proteins, they have the advantage of providing a fast and computationally efficient way to sample equilibrium ensembles and calculate thermodynamic and structural properties under desired conditions. Conformational Monte Carlo techniques employ a move set to perform the transitions in the simulation Markov chain. While accepted conformations must preserve the sequential bonding of the protein chain model and excluded volume among its units, the moves themselves may take the chain across itself. We call this a break in linear topology preservation. In this manuscript, we show, using simple protein models, that there is no difference in equilibrium properties calculated with a move set that preserves linear topology and one that does not. However, for complex structures, such as those of deeply knotted proteins, the preservation of linear topology provides correct equilibrium results but only after long relaxation. In any case, to analyze folding pathways, knotting mechanisms and folding kinetics, the preservation of linear topology may be an unavoidable requirement.

€ Ikusi finantzaketa

Finantzaketari buruzko informazioa

Finantzatzaile

  • FCT, Portugal
    • UID/MULT I/04046/2020
    • SFRH/BD/144345/2019
    • CA17139
    • PID2019-106557GB-C21
  • FCT
    • PTDC/FIS-OUT/28210/2017

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