Flexible Kernels for Protein Property Prediction
Martin Jankowiak, Yerdos Ordabayev, Rudraksh Tuwani, Henry Neil Ward, Hunter Nisonoff, James M McFarland, Gevorg Grigoryan
ICML 2026 regular
Tóm tắt (nguồn: OpenReview · © tác giả)
Despite its importance to applications in protein design, predicting protein properties like binding affinity and thermostability from sparse experimental data remains a significant challenge. Accordingly, we introduce a class of sequence kernels that exploit evolutionary substitution matrices as well as local linearity and demonstrate that the resulting Gaussian processes provide data-efficient models of protein property landscapes, frequently outperforming alternatives that rely on foundation model embeddings. Furthermore--by learning what are in effect structure-aware substitution matrices--we show that our kernels can readily incorporate structural information from foundation models. We demonstrate that these structure-conditioned kernels are well suited to multi-task learning across multiple protein property landscapes and can decisively outperform local supervised learning methods.
Từ khoá
Metadata từ BioTender-max/icml2026-ai-bio (CC0-1.0). Phở không lưu trữ bản PDF; link trỏ về nguồn gốc.
Cùng chủ đề
Chamaileon: Cross-Context Binder Design with Contextualized Modeling and Mixed Sampling
Hengyuan Cao, Shizhuo Cheng, Mingxuan Liu, Weicheng Huang +4
The rapid evolution of generative models has unlocked new potentials in protein binder design, a pivotal task in structural biology, by facilitating end-to-end generation via…
FIDIA: Function-Informed Sequence Design via Inference-Aligned Policy Optimization
Minghan Li, Fengji Li, Yilin Tao, Yue Deng
Computational protein design typically employs a sequential workflow of structure generation followed by sequence (re)design. While structure generators can be explicitly…
FLIP2: Expanding Protein Fitness Landscape Benchmarks for Real-World Machine Learning Applications
Kieran Didi, Sarah Alamdari, Alex Xijie Lu, Bruce James Wittmann +4
Machine learning methods that predict protein fitness from sequence remain sensitive to changes in data distributions, limiting generalization across common conditions encountered…