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bioRxiv · 10.1101/2023.04.20.537604

Pathfinder: protein folding pathway prediction based on conformational sampling

Abstract

The study of protein folding mechanism is a challenge in molecular biology, which is of great significance for revealing the movement rules of biological macromolecules, understanding the pathogenic mechanism of folding diseases, and designing protein engineering materials. Based on the hypothesis that the conformational sampling trajectory contain the information of folding pathway, we propose a protein folding pathway prediction algorithm named Pathfinder. Firstly, Pathfinder performs large-scale sampling of the conformational space and clusters the decoys obtained in the sampling. The heterogeneous conformations obtained by clustering are named seed states. Then, a resampling algorithm that is not constrained by the local energy basin is designed to obtain the transition probabilities of seed states. Finally, protein folding pathways are inferred from the maximum transition probabilities of seed states. The proposed Pathfinder is tested on our developed test set (34 proteins). For 5 widely studied proteins, we correctly predicted their folding pathways. For 25 partial biological experiments proteins, we predicted folding pathways could be further verified. For the other 4 proteins without biological experiment results, potential folding pathways were predicted to provide new insights into protein folding mechanism. The results reveal that structural analogs may have different folding pathways to express different biological functions, homologous proteins may contain common folding pathways, and -helices may be more prone to early protein folding than {beta}-strands.

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BibTeXRIS

Huang, Z., Cui, X., Xia, Y., Zhao, K., Zhang, G.. 2023-04-21. Pathfinder: protein folding pathway prediction based on conformational sampling. https://doi.org/10.1101/2023.04.20.537604

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