Aug 2026· Proceedings of the 32nd ACM SIGKDD Conference on Knowledge Discovery and Data Mining V.2· pp. 12066-12077· 0 citations· 35 references
TL;DR
A function-aware preference alignment framework that improves functional preservation by fine-tuning models to favor function-preserving sequences over function-disrupting alternatives, avoiding the need for explicit function optimization.
Abstract
Protein inverse folding models conditioned on structure achieve high sequence recovery but often fail to preserve biological function due to the lack of functional supervision. We propose a function-aware preference alignment framework that improves functional preservation by fine-tuning models to favor function-preserving sequences over function-disrupting alternatives, avoiding the need for explicit function optimization. Our approach constructs reliable preference pairs in silico using hypothesis-driven perturbations of critical residues and model-consistent likelihood constraints, enabling scalable supervision without additional wet-lab measurements. The resulting framework guides protein sequence design models toward generating sequences that better preserve functional integrity, while remaining compatible with existing inverse folding pipelines such as ProteinMPNN and ESM-IF. Extensive experiments on protein design benchmarks and enzyme datasets with established wet-lab validation show that our fine-tuned models consistently outperform pretrained counterparts in preserving functional integrity during protein sequence design. The code is available at https://github.com/EvaFlower/Function-aware-Protein-Inverse-Folding
This work introduces a symmetric dual-path architecture that both leverages PLMs for pretrained sequence evolution knowledge and MPLMs for pretrained structural knowledge to iteratively guide protein sequence generation.
Han-Dong Wang, Jiaxin Qi, Baisheng Lai et al.· 0 citations
TTS-Design is proposed, a test-time compute scaling framework that enhances protein sequence design without retraining models or relying on larger training datasets, and can consistently improve sequence recovery and structural reliability across different backbone models, without retraining or increasing model size.
Zizhe Jin, Yi Zheng, Huan Yee Koh et al.· Proceedings of the Thirty-Fi...· 0 citations
Inverse FoldDir is a structure-conditioned protein redesign method that combines structural recovery, user control, experimental validation, and a natural route toward future property-guided sampling that performs iterative denoising on the amino acid probability simplex.
Alp Tartici, M. Stojkovic, An-Ru Tian et al.· bioRxiv· 0 citations
ProtLingo, an efficient PLM framework that augments a pretrained single-sequence backbone with conditional local memory and sparse expert routing, achieves competitive performance with a 150M-scale backbone, including strong parameter efficiency on mutation-effect prediction and preserved long-range structural represen...
Ming-Rui Li, Si-Xian Shen, Min-Zhang Li et al.· 0 citations
Multiple sequence alignment (MSA) is a foundational task in computational biology, underpinning protein structure prediction, evolutionary analysis, and domain annotation. Traditional MSA algorithms rely on pairwise amino acid substitution matrices derived from conserved protein families. While effective for aligning c...
Protein fitness prediction is essential for protein engineering. Recent fitness-landscape benchmarks such as FLIP2 have shown that methods performing well under conventional train–test splits can fail when the test set is shifted out of distribution (OOD), including mutations at unseen positions and variants from unsee...