Abstract

In daily life,we are frequently attacked by infection organisms such as bacteria and viruses. Major Histocompatibility (MHC) molecules have an essential role in T-cell activation and initiating an adaptive immune response. Development of methods for prediction of MHC-Peptide binding is important in vaccine design and immunotherapy. In this study, we try to predict the binding between peptides and MHC class II. Support vector machine (SVM) and Multi-Layer Percep-tron (MLP) are used for classification. These classifiers based on pseudo amino acid compositions of data that we ex-tracted from PseAAC server, classify the data. Since, the dataset, used in this work, is imbalanced, we apply a pre-processing step to over-sample the minority class and come over this problem. The results show that using the concept of pseudo amino acid composition and applying over-sampling method, increases the performance of predictor. Fur-thermore, the results demonstrate that using the concept of PseAAC and SVM is a successful method for the prediction of MHC class II molecules.

Highlights

  • Major Histocompatibility (MHC) molecules play a significant role in graft rejection and T-cell activation

  • We try to predict the binding between peptides and MHC class II

  • The results demonstrate that using the concept of PseAAC and Support vector machine (SVM) is a successful method for the prediction of MHC class II molecules

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Summary

Introduction

Major Histocompatibility (MHC) molecules play a significant role in graft rejection and T-cell activation. It is clear that development of machine learning methods to predict the epitopes can reduce the number of the high-cost assay needed to identify T-cell epitopes. We use two machine learning methods to predict the binding between peptide and MHC class II molecule and apply these methods on the HLA-DRB1* 0301 data. In this method, in order to apply machine learning method, peptides with different-lengths are mapped to fixed lengths [3]. In order to apply machine learning method, peptides with different-lengths are mapped to fixed lengths [3]

Generating Chou’s PseAAC
40 Mass and Pk2 and PI
Dataset
Result
Conclusions
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