Classifying the Stoichiometry of Virus-like Particles with Interpretable Machine Learning

Fuente: arXiv
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Autori principali: Zhang, Jiayang, Liu, Xianyuan, Wu, Wei, Tabakhi, Sina, Fan, Wenrui, Zhou, Shuo, Tee, Kang Lan, Wong, Tuck Seng, Lu, Haiping
Natura: Preprint
Pubblicazione: 2025
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author Zhang, Jiayang
Liu, Xianyuan
Wu, Wei
Tabakhi, Sina
Fan, Wenrui
Zhou, Shuo
Tee, Kang Lan
Wong, Tuck Seng
Lu, Haiping
author_facet Zhang, Jiayang
Liu, Xianyuan
Wu, Wei
Tabakhi, Sina
Fan, Wenrui
Zhou, Shuo
Tee, Kang Lan
Wong, Tuck Seng
Lu, Haiping
contents 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.
format Preprint
id arxiv_https___arxiv_org_abs_2502_12049
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Classifying the Stoichiometry of Virus-like Particles with Interpretable Machine Learning
Zhang, Jiayang
Liu, Xianyuan
Wu, Wei
Tabakhi, Sina
Fan, Wenrui
Zhou, Shuo
Tee, Kang Lan
Wong, Tuck Seng
Lu, Haiping
Machine Learning
Biomolecules
Quantitative Methods
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.
title Classifying the Stoichiometry of Virus-like Particles with Interpretable Machine Learning
topic Machine Learning
Biomolecules
Quantitative Methods
url https://arxiv.org/abs/2502.12049