A Deep Learning Framework for Protein-to-Metal Binding Prediction Using Protein Language Models
This study presents an end-to-end deep learning framework for protein-to-metal-ion binding prediction, a critical task in understanding protein function, structural stability, and metal transport mechanisms. A binding site is a residue location in a protein sequence where a metal binds to a protein. Manual curation of metal binding sites is a tedious process involving mining through research articles, making it expensive, laborious, and time-consuming. Therefore, developing a computational pipeline is essential to predict metal ion binding of unannotated proteins. A significant shortcoming of existing computational methods is the failure to capture the long-term dependency of the residues, the absence of positional information, and a pre-determined set of residues and metal ions. In this paper, we propose a metal-ion binding prediction pipeline using a large language model, emphasizing 1) the comparative performance of five state-of-the-art protein language models (pLMs), 2) the impact of positional encoding of binding sites, and 3) the comparison with classical machine learning techniques. A 10-fold cross-validation evaluation yielded a Matthews Correlation Coefficient (MCC) of 0.89, along with precision, recall, and F1 scores exceeding 95% for the six most extensively studied metal ions reported in the literature.
Authors
- Fairuz Shadmani Shishir
- Farzana Rahman (ORCID: https://orcid.org/0000-0002-4785-5845)
- Bishnu Sarker (ORCID: https://orcid.org/0000-0002-9716-4989)
- Sumaiya Shomaji (ORCID: https://orcid.org/0009-0008-9843-2325)
Institutions
- Meharry Medical College (US)
- University of Kansas (US)
- Kingston University London (GB)
- Kingston University (US)
Publication Details
- Journal
- IEEE Transactions on Computational Biology and Bioinformatics
- Published
- 2025-08-11
- DOI
- https://doi.org/10.1109/tcbbio.2025.3595446
- Primary Topic
- Machine Learning in Bioinformatics
- Type
- article
- Field-Weighted Citation Impact
- 0.00