Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering , East China Normal University , Shanghai 200062 , China.
NYU-ECNU Center for Computational Chemistry at NYU Shanghai, Shanghai 200062 , China.
J Chem Inf Model. 2019 Apr 22;59(4):1508-1514. doi: 10.1021/acs.jcim.8b00697. Epub 2019 Feb 25.
Accurately predicting changes in protein stability due to mutations is important for protein engineering and for understanding the functional consequences of missense mutations in proteins. We have developed DeepDDG, a neural network-based method, for use in the prediction of changes in the stability of proteins due to point mutations. The neural network was trained on more than 5700 manually curated experimental data points and was able to obtain a Pearson correlation coefficient of 0.48-0.56 for three independent test sets, which outperformed 11 other methods. Detailed analysis of the input features shows that the solvent accessible surface area of the mutated residue is the most important feature, which suggests that the buried hydrophobic area is the major determinant of protein stability. We expect this method to be useful for large-scale design and engineering of protein stability. The neural network is freely available to academic users at http://protein.org.cn/ddg.html .
准确预测突变引起的蛋白质稳定性变化对于蛋白质工程以及理解蛋白质中错义突变的功能后果非常重要。我们开发了 DeepDDG,一种基于神经网络的方法,用于预测由于点突变引起的蛋白质稳定性变化。该神经网络在 5700 多个经过人工整理的实验数据点上进行了训练,能够为三个独立的测试集获得 0.48-0.56 的皮尔逊相关系数,优于其他 11 种方法。对输入特征的详细分析表明,突变残基的溶剂可及表面积是最重要的特征,这表明埋藏的疏水区是蛋白质稳定性的主要决定因素。我们期望该方法对蛋白质稳定性的大规模设计和工程具有实用价值。该神经网络可供学术用户在 http://protein.org.cn/ddg.html 免费使用。