Protein Folding in the 2D Hydrophobic-Hydrophilic (HP) Square Lattice Model is Chaotic
Jacques M. Bahi, Nathalie C\^ot\'e, Christophe Guyeux, Michel, Salomon

TL;DR
This paper demonstrates that the protein folding process in the 2D HP square lattice model exhibits chaotic dynamics, challenging assumptions of predictability and impacting neural network-based prediction methods.
Contribution
It mathematically proves the chaotic nature of the 2D HP protein folding model and analyzes its complex properties, providing new insights into its unpredictability.
Findings
The 2D HP folding model is a chaotic dynamical system.
Chaotic properties like transitivity and sensitivity are confirmed.
Neural networks struggle to accurately predict the model's evolution.
Abstract
Among the unsolved problems in computational biology, protein folding is one of the most interesting challenges. To study this folding, tools like neural networks and genetic algorithms have received a lot of attention, mainly due to the NP-completeness of the folding process. The background idea that has given rise to the use of these algorithms is obviously that the folding process is predictable. However, this important assumption is disputable as chaotic properties of such a process have been recently highlighted. In this paper, which is an extension of a former work accepted to the 2011 International Joint Conference on Neural Networks (IJCNN11), the topological behavior of a well-known dynamical system used for protein folding prediction is evaluated. It is mathematically established that the folding dynamics in the 2D hydrophobic-hydrophilic (HP) square lattice model, simply…
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Taxonomy
TopicsProtein Structure and Dynamics · Machine Learning in Bioinformatics · Fractal and DNA sequence analysis
