Evidence map›Paper›PMID 42834434›Full record

ArticleBioinformatics (Oxford, England)2026

ParaEM: antigen-aware sequence-based paratope prediction with expectation-maximization.

Taegyu Kim, Changyun Cho, Inuk Jung, Sun Kim

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Taegyu KimInterdisciplinary Program in Artificial Intelligence, Seoul National University, Seoul 08826, Republic of Korea.
Changyun ChoAIGENDRUG Co., Ltd, Seoul 08758, South Korea.
Inuk JungSchool of Computer Science and Engineering, Kyungpook National University, Daegu 41566, Republic of Korea.
Sun KimInterdisciplinary Program in Artificial Intelligence, Seoul National University, Seoul 08826, Republic of Korea.ORCID 0000-0001-5385-9546

Funding

AIGENDRUG CO., LTDArtificial Intelligence Graduate School Program (Seoul National University)]Institute of Information & communications Technology Planning & Evaluation (IITP)Korea government(MSIT) RS-2021-II211343Korea government(MSIT) RS-2023-00257479Korea government(MSIT) RS-2023-NR077172National Research Foundation of Korea (NRF)
6 · The paper itself

Abstract

motivationAccurate identification of antibody paratopes-the residues contacting the antigen-is vital for understanding antibody-antigen recognition, antibody engineering, and vaccine design. However, structure-based predictors require antibody structural inputs, which are often obtained from experimentally determined antibody-antigen complexes in benchmark settings but are generally unavailable for new sequences. Conversely, sequence-based predictors scale efficiently but remain largely antigen-agnostic, limiting their use of pair-specific antigen context.

resultsWe introduce ParaEM, an antigen-aware sequence-based paratope predictor that operates directly on antibody and antigen sequences. ParaEM leverages pretrained ESM3 embeddings to encode both sequences, augmenting antibody residues with trainable, complementarity-determining regions (CDR)-informed embeddings to introduce a biologically informed inductive bias. It models interactions via a residue-level compatibility scorer that defines latent antigen-anchor distributions. During training, a generalized Expectation-Maximization (EM) framework alternates between estimating label-conditioned posterior responsibilities (E-step) and performing gradient-based parameter updates (M-step). Evaluated across three established benchmarks, ParaEM outperforms existing sequence-based baselines in AUC-PR and achieves performance competitive with structure-based predictors without requiring explicit three-dimensional structural inputs. Ablation studies show consistent improvements from generalized EM optimization and an additional gain from CDR-informed embeddings. Antibody-side and antigen-information controls further show that antibody sequence carries substantial predictive signal, while the matching antigen provides additional predictive information. Together, these results support ParaEM as a scalable framework for incorporating matching-antigen context into sequence-based paratope prediction. AVAILABILITY AND IMPLEMENTATION: ParaEM is available at https://github.com/kimtaegyuu/ParaEM. An archival snapshot of the software corresponding to this study is available on Zenodo at DOI: 10.5281/zenodo.22157100.

Indexed as

AntibodiesAntigensComputational BiologySoftwareComplementarity Determining RegionsPrediction AlgorithmsAntibodiesAntigensComplementarity Determining Regions

Identifiers

PMID42834434
PMCPMC13676383

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.