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Epitope prediction algorithms for peptide-based vaccine design

机译:用于基于肽的疫苗设计的表位预测算法

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Peptide-based vaccines, in which small peptides derived from target proteins (epitopes) are used to provoke an immune reaction, have attracted considerable attention recently as a potential means both of treating infectious diseases and promoting the destruction of cancerous cells by a patient's own immune system. With the availability of large sequence databases and computers fast enough for rapid processing of large numbers of peptides, computer aided design of peptide-based vaccines has emerged as a promising approach to screening among billions of possible immune-active peptides to find those likely to provoke an immune response to a particular cell type. In this paper, we describe the development of three novel classes of methods for the prediction of class I epitopes. Each one of the three classes of methods gives a specific set of insights into the epitope prediction problem. We present a quadratic programming approach that can be trained on quantitative as well as qualitative data. The second method uses linear programming to counteract the fact that our training data contains mostly positive examples. The third class of methods uses sequence profiles obtained by clustering known epitopes to score candidate peptides. By integrating these methods, using a simple voting heuristic, we achieve improved accuracy over the state of the art.
机译:近来,基于肽的疫苗被用作治疗传染病和促进患者自身免疫力破坏癌细胞的潜在手段,其中基于靶蛋白(表位)的小肽被用于引发免疫反应。系统。随着大型序列数据库和计算机的快速可用,可以快速处理大量肽,基于计算机的肽疫苗设计已成为一种有前途的方法,可在数十亿种可能的免疫活性肽中进行筛选,从而找到可能引起免疫反应的肽对特定细胞类型的免疫反应。在本文中,我们描述了预测I类表位的三类新颖方法的发展。三种方法中的每一种都提供了对表位预测问题的一组特定见解。我们提出了一种二次编程方法,可以对定量和定性数据进行训练。第二种方法使用线性规划来抵消我们的训练数据主要包含正面示例这一事实。第三类方法使用通过将已知表位聚类而获得的序列图谱来对候选肽进行评分。通过使用简单的投票启发法将这些方法集成在一起,我们可以在现有技术水平上实现更高的准确性。

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