Paper List

期刊: ArXiv Preprint
发布日期: 2025-12-02
BioinformaticsMachine Learning

Few-shot Protein Fitness Prediction via In-context Learning and Test-time Training

Department of Systems Biology, Harvard Medical School | Department of Biology, University of Copenhagen | Machine Intelligence, Novo Nordisk A/S | Microsoft Research, Cambridge, MA, USA | Dept. of Applied Mathematics and Computer Science, Technical University of Denmark

Felix Teufel, Aaron W. Kollasch, Yining Huang, Ole Winther, Kevin K. Yang, Pascal Notin, Debora S. Marks
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IN SHORT: This paper addresses the core challenge of accurately predicting protein fitness with only a handful of experimental observations, where data collection is prohibitively expensive and label availability is severely limited.

核心创新

  • Methodology Introduces PRIMO, a novel transformer-based framework that uniquely combines in-context learning with test-time training for few-shot protein fitness prediction.
  • Methodology Proposes a hybrid masked token reconstruction objective with a preference-based loss function, enabling effective learning from sparse experimental labels across diverse assays.
  • Methodology Develops a lightweight pooling attention mechanism that handles both substitution and indel mutations while maintaining computational efficiency, overcoming limitations of previous methods.

主要结论

  • PRIMO with test-time training (TTT) achieves state-of-the-art few-shot performance, improving from a zero-shot Spearman correlation of 0.51 to 0.67 with 128 shots, outperforming Gaussian Process (0.56) and Ridge Regression (0.63) baselines.
  • The framework demonstrates broad applicability across protein properties including stability (0.77 correlation with TTT), enzymatic activity (0.61), fluorescence (0.30), and binding (0.69), handling both substitution and indel mutations.
  • PRIMO's performance highlights the critical importance of proper data splitting to avoid inflated results, as demonstrated by the 0.4 correlation inflation on RL40A_YEAST when using Metalic's overlapping train-test split.
研究空白： Current methods for protein fitness prediction either require large labeled datasets (supervised approaches) or provide insufficient accuracy (zero-shot methods), and often fail to handle indel mutations or require separate validation sets that exceed practical few-shot budgets.

摘要: Accurately predicting protein fitness with minimal experimental data is a persistent challenge in protein engineering. We introduce PRIMO (PRotein In-context Mutation Oracle), a transformer-based framework that leverages in-context learning and test-time training to adapt rapidly to new proteins and assays without large task-specific datasets. By encoding sequence information, auxiliary zero-shot predictions, and sparse experimental labels from many assays as a unified token set in a pre-training masked-language modeling paradigm, PRIMO learns to prioritize promising variants through a preference-based loss function. Across diverse protein families and properties—including both substitution and indel mutations—PRIMO outperforms zero-shot and fully supervised baselines. This work underscores the power of combining large-scale pre-training with efficient test-time adaptation to tackle challenging protein design tasks where data collection is expensive and label availability is limited.