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Bent, O.

Publications and source records attributed to Bent, O..

2 recordsLinked to original sources

Likelihood-based fine-tuning of protein language models for few-shot fitness prediction and design

Machine learning models trained on measurements of protein functional properties are widely used to accelerate laboratory-based protein design campaigns. To maximise the signal that can be extracted from limited experimental data, sequence embeddings produced by protein language models (PLMs) are often used as the basis of supervised fitness predictors. However, embedding-based predictors do not directly exploit the distributional information encoded in PLM likelihoods after self-supervised or generative pretraining on natural protein sequences. In contrast, likelihood-based fine-tuning approaches exploit this prior knowledge by directly updating pretrained PLM likelihoods to reflect observed fitness differences between sequences. While likelihood-based fine-tuning methods have been proposed previously, a conclusive comparison of their performance against state-of-the-art embedding-based methods has been lacking. To address this gap, we conduct a comprehensive empirical evaluation of both fine-tuning strategies on a representative set of protein fitness datasets from the ProteinGym benchmark. To ensure our evaluation is applicable across different PLM classes, we develop a simple, unified framework for likelihood-based fine-tuning that applies to models trained with various objectives. Across model classes and fitness datasets, likelihood-based fine-tuning consistently outperforms embedding-based methods previously reported as state-of-the-art, with the largest gains in low-data settings. Finally, to highlight the practical relevance of these findings, we demonstrate that the best-performing fine-tuning strategies can substantially improve the maximal fitness of designed sequences in multi-round in silico optimisation campaigns.

bioinformatics↗

Offline RL for generative design of protein binders

Offline Reinforcement Learning (RL) offers a compelling avenue for solving RL problems without the need for interactions with an environment, which may be expensive or unsafe. While online RL methods have found success in various domains, such as de novo Structure-Based Drug Discovery (SBDD), they struggle when it comes to optimizing essential properties derived from protein-ligand docking. The high computational cost associated with the docking process makes it impractical for online RL, which typically requires hundreds of thousands of interactions during learning. In this study, we propose the application of offline RL to address the bottleneck posed by the docking process, leveraging RLs capability to optimize non-differentiable properties. Our preliminary investigation focuses on using offline RL to conditionally generate drugs with improved docking and chemical properties.

bioinformatics↗