Sep 2026· Proceedings of the Thirty-Fifth International Joint Conference on Artificial Intelligence· 0 citations· 27 references
TL;DR
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.
Abstract
Generating protein sequences that reliably fold into target structures is a central challenge in computational biology and protein design. Progress in protein inverse folding (PIF), however, is fundamentally constrained by the scarcity of high-quality structural data, which limits the effectiveness of existing models. In this work, we propose TTS-Design, a test-time compute scaling framework that enhances protein sequence design without retraining models or relying on larger training data. For TTS-Design, its core design is a dedicated inverse folding reward model named IF-RM, which quantitatively evaluates structure–sequence compatibility and enables effective selection among multiple candidate sequences at inference time. By integrating IF-RM into existing PIF models, TTS-Design leverages additional computation during inference stage to explore and refine candidate solutions. Extensive experiments on the CATH 4.2 and CATH 4.3 demonstrate that TTS-Design consistently improves sequence recovery and structural reliability across different backbone models, without retraining or increasing model size. Case studies on real-world proteins further confirm its practical effectiveness. Overall, our results highlight test-time compute scaling as a promising and effective paradigm for advancing protein inverse folding and other scientific problems under data-limited scenarios.
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-preser...
Nilufer Tamatgar, Soobin Park, Yinghua Yao et al.· Proceedings of the 32nd ACM...· 0 citations
OpenDDE is introduced, an open-source, all-atom biomolecular foundation model that uses co-folding as the entry point to a scalable AI-driven drug discovery engine and identifies two scaling-law directions for co-folding models.
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Dingyi Rong, Haotian Lu, Xupeng Zhang et al.· Journal of Chemical Informat...· 0 citations
This mini review traces the evolution of AI-driven methods in protein research, from early residue-contact prediction using coevolutionary information to transformative breakthroughs, the rise of protein language models (PLMs), and the emerging era of generative design and functional modeling.
Guodong Min, Huan Peng· Methods in molecular biology· 0 citations
It is shown that accurate ΔTm prediction does not require structural input features, but can achieve state-of-the-art results with a careful training design for large sequence-based protein language models, and choices such as loss function, pooling strategy, auxiliary supervision, and finetuning regime materially affe...
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AgentFold is presented, a multi-agent framework that formulates folding-model development as a closed-loop search over executable code variants and improves the best lDDT by 7.5% over independent Codex proposals and outperforms a random-search control.
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