SESNet: sequence-structure feature-integrated deep learning method for data-efficient protein engineering

• URL: http://arxiv.org/abs/2301.00004v1
• Date: Thu, 29 Dec 2022 01:49:52 GMT
• Title: SESNet: sequence-structure feature-integrated deep learning method for data-efficient protein engineering
• Authors: Mingchen Li, Liqi Kang, Yi Xiong, Yu Guang Wang, Guisheng Fan, Pan Tan, Liang Hong
• Abstract summary: We develop SESNet, a supervised deep-learning model to predict the fitness for protein mutants. We show that SESNet outperforms state-of-the-art models for predicting the sequence-function relationship. Our model can achieve strikingly high accuracy in prediction of the fitness of protein mutants, especially for the higher order variants.
• Score: 6.216757583450049
• License: http://creativecommons.org/licenses/by-nc-sa/4.0/
• Abstract: Deep learning has been widely used for protein engineering. However, it is limited by the lack of sufficient experimental data to train an accurate model for predicting the functional fitness of high-order mutants. Here, we develop SESNet, a supervised deep-learning model to predict the fitness for protein mutants by leveraging both sequence and structure information, and exploiting attention mechanism. Our model integrates local evolutionary context from homologous sequences, the global evolutionary context encoding rich semantic from the universal protein sequence space and the structure information accounting for the microenvironment around each residue in a protein. We show that SESNet outperforms state-of-the-art models for predicting the sequence-function relationship on 26 deep mutational scanning datasets. More importantly, we propose a data augmentation strategy by leveraging the data from unsupervised models to pre-train our model. After that, our model can achieve strikingly high accuracy in prediction of the fitness of protein mutants, especially for the higher order variants (> 4 mutation sites), when finetuned by using only a small number of experimental mutation data (<50). The strategy proposed is of great practical value as the required experimental effort, i.e., producing a few tens of experimental mutation data on a given protein, is generally affordable by an ordinary biochemical group and can be applied on almost any protein.

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