Predicting Protein Subcellular Localizations for Gram-Negative Bacteria Using DP-PSSM and Support Vector Machines

Eric Y. T. Juan, W. J. Li, J. Jhang, C. Chiu
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引用次数: 11

Abstract

Invisible bacteria are found almost everywhere, and having a great impact on our everyday life. Particularly, many species of gram-negative bacteria are pathogenic and cause a wide variety of diseases in humans and animals. It is crucial in drug design to cure diseases brought by gram-negative bacteria. Unfortunately, a new drug discovery can be expensive and time-consuming even with the advance of biotechnology. Designing a highly effective and efficient computational system, especially for identifying protein subcellular localization for gram-negative bacteria, is an important research field.In this paper, we propose a new computational system which combines a well-known classifier, support vector machines (SVMs), a protein descriptor, DP-PSSM (Directional Property-PSSM), and an optimal tool for system tuning. In addition, an evolutionary computation based feature selection technique is applied to further improve the performance of our computational system. Our computational system, EF-SVM-PSL, had been tested through 10 fold cross validation on predicting subcellular localizations of three gram-negative bacteria protein datasets, PS1444, NR828, and EV243. Our EF-SVM-PSL has a relative simple architecture and performs competitively with the best alternative systems.
利用DP-PSSM和支持向量机预测革兰氏阴性菌的蛋白质亚细胞定位
看不见的细菌几乎无处不在,对我们的日常生活有很大的影响。特别是,许多革兰氏阴性菌是致病性的,并在人类和动物中引起各种各样的疾病。治疗革兰氏阴性菌引起的疾病是药物设计的关键。不幸的是,即使在生物技术进步的情况下,一种新药的发现也可能是昂贵和耗时的。设计一个高效的计算系统,特别是用于革兰氏阴性菌的蛋白质亚细胞定位,是一个重要的研究领域。在本文中,我们提出了一个新的计算系统,它结合了一个著名的分类器、支持向量机(svm)、蛋白质描述符DP-PSSM (Directional Property-PSSM)和一个最优的系统调优工具。此外,还采用了一种基于进化计算的特征选择技术,进一步提高了计算系统的性能。我们的计算系统EF-SVM-PSL在预测三个革兰氏阴性菌蛋白数据集(PS1444、NR828和EV243)的亚细胞定位方面进行了10倍交叉验证。我们的EF-SVM-PSL具有相对简单的体系结构,并且与最佳替代系统相比具有竞争力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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