Prediction of mutation-induced protein stability changes based on the geometric representations learned by a self-supervised method

Autor: Shan Shan Li, Zhao Ming Liu, Jiao Li, Yi Bo Ma, Ze Yuan Dong, Jun Wei Hou, Fu Jie Shen, Wei Bu Wang, Qi Ming Li, Ji Guo Su
Jazyk: angličtina
Rok vydání: 2024
Předmět:
Zdroj: BMC Bioinformatics, Vol 25, Iss 1, Pp 1-19 (2024)
Druh dokumentu: article
ISSN: 1471-2105
DOI: 10.1186/s12859-024-05876-6
Popis: Abstract Background Thermostability is a fundamental property of proteins to maintain their biological functions. Predicting protein stability changes upon mutation is important for our understanding protein structure–function relationship, and is also of great interest in protein engineering and pharmaceutical design. Results Here we present mutDDG-SSM, a deep learning-based framework that uses the geometric representations encoded in protein structure to predict the mutation-induced protein stability changes. mutDDG-SSM consists of two parts: a graph attention network-based protein structural feature extractor that is trained with a self-supervised learning scheme using large-scale high-resolution protein structures, and an eXtreme Gradient Boosting model-based stability change predictor with an advantage of alleviating overfitting problem. The performance of mutDDG-SSM was tested on several widely-used independent datasets. Then, myoglobin and p53 were used as case studies to illustrate the effectiveness of the model in predicting protein stability changes upon mutations. Our results show that mutDDG-SSM achieved high performance in estimating the effects of mutations on protein stability. In addition, mutDDG-SSM exhibited good unbiasedness, where the prediction accuracy on the inverse mutations is as well as that on the direct mutations. Conclusion Meaningful features can be extracted from our pre-trained model to build downstream tasks and our model may serve as a valuable tool for protein engineering and drug design.
Databáze: Directory of Open Access Journals
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