eSIG-Net: Accurate prediction of single-mutation induced perturbations on protein interactions using a language model
Year: 2026
Type: preprint
Abstract: Most proteins exert their functions in complex with other interactors. Single mutations can exhibit a profound impact on perturbing protein interactions, leading to human disease. However, predicting the effect of single mutations on protein interactions remains a major computational challenge. Deep learning, particularly protein language models or transformers, has become an effective tool in bioinformatics for protein structure prediction. However, the functional divergence of mutations makes it difficult to predict their interaction perturbation profiles. To address this fundamental challenge, we present eSIG-Net (edgetic mutation Sequence-based Interaction Grammar Network), a novel sequence-based “Interaction Language Model” for predicting protein interaction alterations caused by single mutations. eSIG-Net combines various protein sequence embeddings, introduces a mutation-encoding module with syntax and evolutionary insights, and employs contrastive learning to evaluate mutation-induced interaction changes. eSIG-Net significantly outperforms current state-of-the-art sequence-based and structure-based prediction methods at predicting mutational impact on protein interactions. We highlight examples where eSIG-Net nominates causal variants with high confidence and elucidates their functional role under relevant biological contexts. Together, eSIG-Net is a first-in-kind “interaction language model” that can accurately predict interaction-specific rewiring by single mutations with only sequence information, and exhibits generalizability across biological contexts.
Institutions: Baylor College of Medicine, The University of Texas at Austin, Case Western Reserve University, Yale Cancer Center, Yale University, The University of Texas Health Science Center at Houston, Dan L Duncan Comprehensive Cancer Center, Texas A&M University, Boston University, Dana-Farber Cancer Institute, Stanford Medicine, Stanford University, Cleveland Clinic, University of Virginia Cancer Center, University of Virginia
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Awards: PREDICTING RESPONSE TO TREATMENT IN SYSTEMIC SCLEROSIS-RELATED INTERSTITIAL LUNG DISEASE IN A MULTICENTER OBSERVATIONAL COHORT, G4119534169, G4182736573, G510513728, Engagement and outreach to achieve a FAIR data ecosystem for the BICAN, G5850682332, G6034815006, G9000005305, G9000012654, G9000076341, Mechanisms of Action of Natural Genetic Variation, Baylor College of Medicine Cancer Center - Cancer Center Support Grant, An integrated functional proteomics platform for accelerated discovery of isoform-specific determinants of cancer
OpenAlex ID: W7143962955
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