期刊
BIOINFORMATICS
卷 34, 期 13, 页码 274-283出版社
OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/bty238
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资金
- Academy of Finland Center of Excellence in Systems Immunology and Physiology
- Academy of Finland [260403, 299915]
- Finnish Funding Agency for Innovation Tekes [40128/14]
- Academy of Finland (AKA) [260403, 299915, 299915, 260403] Funding Source: Academy of Finland (AKA)
Motivation: Proteins are commonly used by biochemical industry for numerous processes. Refining these proteins' properties via mutations causes stability effects as well. Accurate computational method to predict how mutations affect protein stability is necessary to facilitate efficient protein design. However, accuracy of predictive models is ultimately constrained by the limited availability of experimental data. Results: We have developed mGPfusion, a novel Gaussian process (GP) method for predicting protein's stability changes upon single and multiple mutations. This method complements the limited experimental data with large amounts of molecular simulation data. We introduce a Bayesian data fusion model that re-calibrates the experimental and in silico data sources and then learns a predictive GP model from the combined data. Our protein-specific model requires experimental data only regarding the protein of interest and performs well even with few experimental measurements. The mGPfusion models proteins by contact maps and infers the stability effects caused by mutations with a mixture of graph kernels. Our results show that mGPfusion outperforms stateof-the-art methods in predicting protein stability on a dataset of 15 different proteins and that incorporating molecular simulation data improves the model learning and prediction accuracy.
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