Evidence map›Paper›PMID 42412784›Full record

ArticleBioinformatics (Oxford, England)2026

USP-ddG: a unified structural paradigm with data efficacy and mixture-of-experts for predicting mutational effects on protein-protein interactions.

Guanglei Yu, Xuehua Bi, Qichang Zhao, Jianxin Wang

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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.

Guanglei YuSchool of Computer Science and Engineering, Central South University, Changsha 410083, China.
Xuehua BiCollege of Medical Engineering and Technology, Xinjiang Medical University, Urumqi 830017, China.
Qichang ZhaoSchool of Computer Science and Engineering, Central South University, Changsha 410083, China.ORCID 0000-0002-8319-9793
Jianxin WangSchool of Computer Science and Engineering, Central South University, Changsha 410083, China.ORCID 0000-0003-1516-0480

Funding

High Performance Computing Center of Central South UniversityNational Natural Science Foundation of China 62332020Xiangjiang Laboratory 23XJ01011
6 · The paper itself

Abstract

motivationAccurately estimating changes in binding free energy (ΔΔG) is critical for understanding protein-protein interactions (PPIs) and guiding rational protein design. Recent deep learning methods have achieved notable progress by pre-training on large-scale structural data. While some approaches explore structural flexibility through energy-based sampling or generative modeling, these strategies typically involve substantial computational cost and overlook data efficacy in terms of training data organization.

resultsWe present USP-ddG, a unified structural paradigm for ΔΔG prediction built on a dual-channel architecture. The model incorporates three complementary components: (i) an inverse folding-based log-odds ratio, (ii) the empirical force field FoldX capturing side-chain packing energetics, and (iii) a geometric encoder that leverages Gaussian coordinate perturbation as a regularization strategy to improve robustness. To enhance representation capacity, we introduce a framework that integrates feed-forward network (FFN) and Mixture-of-Experts (MoE) to model domain-invariant and -specific features, respectively. We further propose CATH-guided Folding Ordering (CFO), a data efficacy strategy that organizes samples to mitigate catastrophic forgetting and data distribution bias. USP-ddG consistently outperforms existing state-of-the-art methods on the SKEMPI v2.0 benchmark, including the challenging hold-out CATH test set. It achieves superior accuracy on both single- and multi-point mutations and demonstrates strong performance in antibody affinity optimization against H1N1 and HER2, and in predicting the impact of SARS-CoV-2 variants on hACE2 binding. Ablation studies confirm the contribution of each component. These results highlight USP-ddG as a robust and data-efficient framework for modeling mutational effects on PPIs. AVAILABILITY AND IMPLEMENTATION: USP-ddG is available at https://github.com/ak422/USP-ddG.

Indexed as

Computational BiologyMutationProtein Interaction MappingProteinsDeep LearningProtein BindingThermodynamicsProteins

Identifiers

PMID42412784
PMCPMC13340161

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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.