Kang Shuli, Chen Gang, Xiao Gengfu
State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, Hubei 430072, China.
Protein Eng Des Sel. 2009 Feb;22(2):75-83. doi: 10.1093/protein/gzn063. Epub 2008 Dec 2.
Current methods of predicting mutation-induced protein stability change are imprecise. Machine learning methods have been introduced for this prediction recently; however, the available experimental data used for training these predictors are biased. Abundant data are available for several frequently occurring amino acid substitutions, whereas only limited data have been accumulated for some other mutation types. Generally, current statistical models do not account for this bias toward the commoner amino acids during the encoding process and are thus less effective in making predictions on less frequently occurring mutations. In this paper, we propose a method based on support vector machines and property encoding of amino acids. The predictor we constructed outperforms other methods on the same data sets and is more robust with poor training data. The prediction accuracy for mutations with no training data exceeded 80%. This advantage is critical for practical application, where the prediction could be applied for any type of mutations. Further analysis demonstrates our model relies on biological significant features to make predictions. To overcome the drawbacks of classifying mutations into 'stabilizing' and 'destabilizing' ones, a three-class classification of mutations was also discussed, where our method obtained an overall accuracy of 79.1%.
目前预测突变引起的蛋白质稳定性变化的方法并不精确。机器学习方法最近已被引入用于这种预测;然而,用于训练这些预测器的现有实验数据存在偏差。对于几种常见的氨基酸替换有大量数据,而对于其他一些突变类型仅积累了有限的数据。一般来说,当前的统计模型在编码过程中没有考虑到对较常见氨基酸的这种偏差,因此在对较少出现的突变进行预测时效果较差。在本文中,我们提出了一种基于支持向量机和氨基酸性质编码的方法。我们构建的预测器在相同数据集上优于其他方法,并且在训练数据较差时更稳健。对于没有训练数据的突变,预测准确率超过80%。这一优势对于实际应用至关重要,在实际应用中该预测可应用于任何类型的突变。进一步分析表明我们的模型依赖于生物学上有意义的特征来进行预测。为了克服将突变分为“稳定化”和“去稳定化”突变的缺点,还讨论了突变的三类分类,我们的方法在其中获得了79.1%的总体准确率。