Abstract

This study concerns an attempt to establish a new method for predicting antimicrobial peptides (AMPs) which are important to the immune system. Recently, researchers are interested in designing alternative drugs based on AMPs because they have found that a large number of bacterial strains have become resistant to available antibiotics. However, researchers have encountered obstacles in the AMPs designing process as experiments to extract AMPs from protein sequences are costly and require a long set-up time. Therefore, a computational tool for AMPs prediction is needed to resolve this problem. In this study, an integrated algorithm is newly introduced to predict AMPs by integrating sequence alignment and support vector machine- (SVM-) LZ complexity pairwise algorithm. It was observed that, when all sequences in the training set are used, the sensitivity of the proposed algorithm is 95.28% in jackknife test and 87.59% in independent test, while the sensitivity obtained for jackknife test and independent test is 88.74% and 78.70%, respectively, when only the sequences that has less than 70% similarity are used. Applying the proposed algorithm may allow researchers to effectively predict AMPs from unknown protein peptide sequences with higher sensitivity.

Highlights

  • Antimicrobial peptides (AMPs) have been used in drug design to fight many types of microorganisms such as bacteria, fungi, parasites, enveloped viruses, and cancer cells [1]

  • The proposed algorithm was the combination of the sequence alignment method and support vector machine- (SVM-)LZ complexity pairwise algorithm

  • In the support vector machine (SVM)-LZ complexity pairwise algorithm, the peptide sequences were represented by the fixed length feature vectors

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Summary

Introduction

Antimicrobial peptides (AMPs) have been used in drug design to fight many types of microorganisms such as bacteria, fungi, parasites, enveloped viruses, and cancer cells [1]. AMPs kill microorganisms through disruption of membrane integrity and are believed to be less likely to induce resistance [2]. AMPs are a group of molecules that form an important part of the innate immune system. AMPs consist of 12 to 100 amino acid residues and can be found among all classes of life including bacteria, fungi, plants, invertebrates, and vertebrates [3, 4]. By referring to their activities, structural properties, and sequence features, AMPs can be classified into several main categories such as antibacterial, antifungal, antiviral, antitumor and anticancer [5, 6]

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