BindPred: A Framework for Predicting Protein-Protein Binding Affinity from Language Model Embeddings
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Motivation
Reliable predictions of protein–protein binding affinities are essential for molecular biology and therapeutic discovery. However, most computational methods rely on three-dimensional structural models, which are often unavailable for many complexes.
Results
We introduce BindPred, a structure-agnostic input framework that predicts affinities directly from amino acid sequences by combining embeddings from large protein language models with gradient boosting trees. On the PPB-Affinity benchmark, which comprises 11,919 diverse complexes, BindPred achieves a Pearson correlation coefficient of 0.86 in random split five-fold cross-validation, where the training and test sets share <30% global sequence identity. Ablation analysis indicates that evolutionary embeddings alone capture most of the predictive signals, while augmenting with physics-based energy terms from PyRosetta and BindCraft increases the correlation by only 0.01. A more stringent protein-level split that places entire protein families (wild-type and all mutants) exclusively in either training or testing sets, results in only a modest decline in performance, demonstrating robust generalization to novel interaction pairs. Because BindPred operates exclusively on sequence input, it enables rapid inference (approximately 3 million complexes per GPU (T4) hour), making proteome-scale screening computationally feasible.
Availability
The pretrained model and inference pipeline are available in a Google Colab notebook: BindPred Colab notebook . The training dataset, code, and model weights are available on the Hugging Face: BindPred
Contact
costas@psu.edu
Supplementary information
Supplementary data are available at Bioinformatics online.
