摘要
Protein-protein interactions (PPIs) perform a very important function in a number of cellular processes, including signal transduction, post-translational modifications, apoptosis, and cell growth. Deregulation of PPIs will lead to many diseases, including pernicious anemia or cancers. Although a large number of high-throughput techniques are designed to generate PPIs data, they are generally expensive, inefficient, and labor-intensive. Hence, there is an urgent need for developing a computational method to accurately and rapidly detect PPIs. In this article, we proposed a highly efficient method to detect PPIs by integrating a new protein sequence sub-stitution matrix feature representation and ensemble weighted sparse representation model classifier. The proposed method is demonstrated on Saccharomyces cerevisiae dataset and achieved 99.26 percent prediction accuracy with 98.53 percent sensitivity at precision of 100 percent, which is shown to have much higher predictive accuracy than the state-of-the-art methods. Extensive contrast experiments are performed with the benchmark data set from Human and Helicobacter pylori that our proposed method can achieve outstanding better success rates than other existing approaches in this problem. Experiment results illustrate that our proposed method presents an economical approach for computational building of PPI networks, which can be a helpful supplementary method for future proteomics researches.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 8540898 |
| 页(从-至) | 809-817 |
| 页数 | 9 |
| 期刊 | IEEE/ACM Transactions on Computational Biology and Bioinformatics |
| 卷 | 16 |
| 期 | 3 |
| DOI | |
| 出版状态 | 已出版 - 1 5月 2019 |
| 已对外发布 | 是 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 3 良好健康与福祉
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