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Biology subjects

Vithayapalert, N.

Publications and source records attributed to Vithayapalert, N..

2 recordsLinked to original sources

Generalizing Protein Fitness Prediction Across Distribution Shifts via Structural and Co-evolutionary Priors

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 unseen protein backbones. In particular, current protein language models (pLMs) often suffer substantial performance degradation under such distribution shifts, limiting their practical use in protein engineering. We therefore develop a framework that augments sequence representations with structural and co-evolutionary information for fitness prediction. Specifically, we pair structure-aware pLMs with features pooled from an AlphaFold-style trunk applied to each sequence and its multiple sequence alignment (MSA), and use a lightweight prediction probe to map these frozen representations to fitness scores. Our framework consistently outperforms the best previously reported FLIP2 scores across several types of distribution shift. We then systematically study the contribution of each component in our framework to generalization. Structural priors yield the largest performance gains on held-out protein backbones, whereas trunk features improve generalization to held-out mutation positions. Rather than proposing a single best method, we characterize which modalities are effective for different protein families and distribution shifts, providing practical guidance for choosing representations according to the generalization regime. These findings support the development of more generalizable fitness predictors that can serve as effective reward functions or oracles for protein design toward desired functions.

bioengineering↗

Towards Generalizable Protein-ligand Co-folding with ACER

Predicting protein-ligand complex structures is a central challenge in drug discovery. While recent co-folding models such as AlphaFold-3 achieve accurate structure prediction, they fail to generalize to underexplored binding interfaces - systematically misplacing ligands, particularly for allosteric or structurally novel targets. To address this gap, we present ACER (Adaptive Co-folding via pocket Exploration and pose Ranking), a training-free framework that (a) enables co-folding models to systematically explore alternative binding pockets, and (b) leverages the discovered pockets to increase pose accuracy. Our method enables the efficient discovery of non-prevalent pockets without prior expert knowledge. ACER improves pocket discovery and pose accuracy on allosteric targets and structurally novel complexes, successfully modeling binding interfaces that are under-represented or absent from the training set. Our results demonstrate how improved sampling dynamics enhance the generalisability of co-folding models without retraining.

bioinformatics↗