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Classifying the Stoichiometry of Virus-like Particles with Interpretable Machine Learning
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Virus-like particles (VLPs) are valuable for vaccine development due to their immune-triggering properties. Understanding their stoichiometry, the number of protein subunits to form a VLP, is critical for vaccine optimisation. However, current experimental methods to determine stoichiometry are time-consuming and require highly purified proteins. To efficiently classify stoichiometry classes in proteins, we curate a new dataset and propose an interpretable, data-driven pipeline leveraging linear machine learning models. We also explore the impact of feature encoding on model performance and interpretability, as well as methods to identify key protein sequence features influencing classification. The evaluation of our pipeline demonstrates that it can classify stoichiometry while revealing protein features that possibly influence VLP assembly. The data and code used in this work are publicly available at https://github.com/Shef-AIRE/StoicIML.
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Topological Learning Prediction of Virus-like Particle Stoichiometry and Stability
Persistent Laplacian features predict VLP stoichiometry with reported AUC up to 0.98, but the stability conclusion rests on classifier accuracy rather than physical stability, and the input features may leak the label.
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