Leveraging ancestral sequence reconstruction for protein representation learning

被引:1
|
作者
Matthews, D.S. [1 ,2 ]
Spence, M.A. [1 ,2 ]
Mater, A.C. [1 ]
Nichols, J. [3 ]
Pulsford, S.B. [1 ,4 ]
Sandhu, M. [1 ]
Kaczmarski, J.A. [3 ,4 ]
Miton, C.M. [5 ]
Tokuriki, N. [5 ]
Jackson, C.J. [1 ,2 ,3 ,4 ]
机构
[1] Research School of Chemistry, Australian National University, Canberra,ACT, Australia
[2] ARC Centre for Innovations in Peptide and Protein Science, Australian National University, Canberra,ACT, Australia
[3] Research School of Biology, Australian National University, Canberra,ACT, Australia
[4] ARC Centre of Excellence in Synthetic Biology, Australian National University, Canberra,ACT, Australia
[5] Michael Smith Laboratories, University of British Columbia, Vancouver,BC, Canada
关键词
Protein language models (PLMs) convert amino acid sequences into the numerical representations required to train machine learning models. Many PLMs are large (>600 million parameters) and trained on a broad span of protein sequence space. However; these models have limitations in terms of predictive accuracy and computational cost. Here we use multiplexed ancestral sequence reconstruction to generate small but focused functional protein sequence datasets for PLM training. Compared to large PLMs; this local ancestral sequence embedding produces representations with higher predictive accuracy. We show that due to the evolutionary nature of the ancestral sequence reconstruction data; local ancestral sequence embedding produces smoother fitness landscapes; in which protein variants that are closer in fitness value become numerically closer in representation space. This work contributes to the implementation of machine learning-based protein design in real-world settings; where data are sparse and computational resources are limited. © The Author(s); under exclusive licence to Springer Nature Limited 2024;
D O I
10.1038/s42256-024-00935-2
中图分类号
学科分类号
摘要
Protein language models (PLMs) convert amino acid sequences into the numerical representations required to train machine learning models. Many PLMs are large (>600 million parameters) and trained on a broad span of protein sequence space. However, these models have limitations in terms of predictive accuracy and computational cost. Here we use multiplexed ancestral sequence reconstruction to generate small but focused functional protein sequence datasets for PLM training. Compared to large PLMs, this local ancestral sequence embedding produces representations with higher predictive accuracy. We show that due to the evolutionary nature of the ancestral sequence reconstruction data, local ancestral sequence embedding produces smoother fitness landscapes, in which protein variants that are closer in fitness value become numerically closer in representation space. This work contributes to the implementation of machine learning-based protein design in real-world settings, where data are sparse and computational resources are limited.
引用
收藏
页码:1542 / 1555
页数:13
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