Sign in
BioinformaticsbioRxiv
Preprint

PREpiBind: Protein Representation-integrated Epitope-MHC Class II Binding Prediction

David Hyunyoo JangiD, 황운택, Dongwoo KimiD, Byungho ParkiD, Yoonjoo ChoiiD, Juyong LeeiD

Abstract

Motivation: Accurate peptide-MHC class II (pMHC-II) binding prediction is complicated by MHC polymorphism and context-dependent peptide recognition. Protein representations are usually evaluated in different pipelines, obscuring their contribution to predictive performance. Results: We present PREpiBind, a joint-attention framework comparing ten protein representations under a fixed architecture and identical data splits across qualitative binding, mass spectrometry, and thresholded IC50 datasets. PLMs generally achieved the strongest pooled performance; ESM3 Large reached a ROC-AUC of 0.927 +/- 0.002 on the qualitative dataset. PREpiBind PLM variants exceeded evaluated reference methods on qualitative and mass-spectrometry benchmarks, whereas NetMHCIIpan-4.3 was higher on thresholded IC50 using its binding-affinity head. PLM advantages narrowed in allele-wise and held-out MHC-molecule evaluations, and H2-out rankings depended on aggregation, indicating scenario-dependent representation performance. Availability and implementation: Source code and the training and evaluation datasets are available at https://github.com/daylight-00/PREpiBind and archived at https://doi.org/10.5281/zenodo.22934281; trained model checkpoints are available at https://huggingface.co/daylight-00/prepibind. Implemented in Python and released under the MIT License. Contact: nicole23@snu.ac.kr Supplementary information: Supplementary data are available online.

PDFDOICode

02 /Specification & Classification

Click any tag to browse matching papers

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.