AI Article Synopsis

  • Protein methylation is crucial for various biological functions, but there is a growing gap between known protein sequences and their methylation annotations, emphasizing the need for better identification methods.
  • A new computational tool called Methy_SVMIACO is developed, combining support vector machine (SVM) and improved ant colony optimization (IACO) to accurately identify methylation sites by optimizing SVM parameters.
  • Methy_SVMIACO shows strong performance with high sensitivity, specificity, and accuracy for both lysine and arginine methylation, outperforming existing methods and highlighting the significance of surrounding residues in the methylation process.

Article Abstract

Protein methylation is involved in dozens of biological processes and plays an important role in adjusting protein physicochemical properties, conformation and function. However, with the rapid increase of protein sequence entering into databanks, the gap between the number of known sequence and the number of known methylation annotation is widening rapidly. Therefore, it is vitally significant to develop a computational method for quick and accurate identification of methylation sites. In this study, a novel predictor (Methy_SVMIACO) based on support vector machine (SVM) and improved ant colony optimization algorithm (IACO) is developed to identify methylation sites. The IACO is utilized to find the optimal feature subset and parameter of SVM, while SVM is employed to perform the identification of methylation sites. Comparison of the IACO with conventional ACO shows that the IACO converges quickly toward the global optimal solution and it is more useful tool for feature selection and SVM parameter optimization. The performance of Methy_SVMIACO is evaluated with a sensitivity of 85.71%, a specificity of 86.67%, an accuracy of 86.19% and a Matthew's correlation coefficient (MCC) of 0.7238 for lysine as well as a sensitivity of 89.08%, a specificity of 94.07%, an accuracy of 91.56% and a MCC of 0.8323 for arginine in 10-fold cross-validation test. It is shown through the analysis of the optimal feature subset that some upstream and downstream residues play important role in the methylation of arginine and lysine. Compared with other existing methods, the Methy_SVMIACO provides higher Acc, Sen and Spe, indicating that the current method may serve as a powerful complementary tool to other existing approaches in this area. The Methy_SVMIACO can be acquired freely on request from the authors.

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http://dx.doi.org/10.1016/j.aca.2011.08.008DOI Listing

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