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This research introduces VenusREM-Harness, a model-agnostic framework that integrates evolutionary evidence and structural context to correct biases in protein foundation models. By fusing frozen model scores with multiple sequence alignment data, the approach significantly improves fitness prediction accuracy across diverse benchmarks without requiring retraining. This advancement addresses critical limitations in current deep learning tools for protein engineering by providing more reliable sequence-function relationships.
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A General Harness for Protein Foundation Model Fitness Prediction

arXiv2 min de cititArticolul și perspectiva sunt în engleză.

arXiv:2609.34654v1 Announce Type: new Abstract: Accurate fitness prediction is central to protein engineering and understanding sequence-function relationships. With advances in deep learning, protein foundation models (PFMs) have become widely used for this task. Recent analyses, however, show that these models share preferences reflecting their training corpora, while unreliable inputs can further distort fitness predictions. Family-specific evolutionary evidence and structural context can help address these limitations by providing complementary constraints on model scores, motivating VenusREM-Harness (VRH), a general, model-agnostic, training-free Retrieval-Enhanced Mutation harness. It fuses frozen model scores with multiple sequence alignment (MSA) evidence according to model uncertainty, then applies gated background correction and score shrinkage based on structural confidence and solvent exposure. Across 1,211 assays and 3.1 million measured variants from ProteinGym, VenusMutHub, and the newly curated viral benchmark VenusViroHub, all 71 configurations improve Spearman correlation on all 3 benchmarks by 0.073 on average, with broad gains across 5 metrics. Extended analyses relate retrieval gains to model-MSA preference differences, assess domain-level gains and immune-escape cases, and quantify computational speedups. Built with VRH, VenusREM2 is the first to rank highest in all function, taxon, MSA-depth, and mutation-depth categories, with a ProteinGym Average Spearman of 0.556, 0.038 above the prior best.

Abstract:Accurate fitness prediction is central to protein engineering and understanding sequence-function relationships. With advances in deep learning, protein foundation models (PFMs) have become widely used for this task. Recent analyses, however, show that these models share preferences reflecting their training corpora, while unreliable inputs can further distort fitness predictions. Family-specific evolutionary evidence and structural context can help address these limitations by providing complementary constraints on model scores, motivating VenusREM-Harness (VRH), a general, model-agnostic, training-free Retrieval-Enhanced Mutation harness. It fuses frozen model scores with multiple sequence alignment (MSA) evidence according to model uncertainty, then applies gated background correction and score shrinkage based on structural confidence and solvent exposure. Across 1,211 assays and 3.1 million measured variants from ProteinGym, VenusMutHub, and the newly curated viral benchmark VenusViroHub, all 71 configurations improve Spearman correlation on all 3 benchmarks by 0.073 on average, with broad gains across 5 metrics. Extended analyses relate retrieval gains to model-MSA preference differences, assess domain-level gains and immune-escape cases, and quantify computational speedups. Built with VRH, VenusREM2 is the first to rank highest in all function, taxon, MSA-depth, and mutation-depth categories, with a ProteinGym Average Spearman of 0.556, 0.038 above the prior best.

Artificial Intelligence (cs.AI); Quantitative Methods (q-bio.QM)

arXiv:2609.34654 [cs.AI]

(or arXiv:2609.34654v1 [cs.AI] for this version)

https://doi.org/10.48550/arXiv.2609.34654 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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