Quantitative Prediction of Linear B-Cell Epitopes

R. Isea
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引用次数: 7

Abstract

In scientific literature, there are many programs that predict linear B-cell epitopes from a protein sequence. Each program generates multiple B-cell epitopes that can be individually studied. This paper defines a function called that combines results from five different prediction programs concerning the linear B-cell epitopes (ie., BebiPred, EPMLR, BCPred, ABCPred and Emini Prediction) for selecting the best B-cell epitopes. We obtained 17 potential linear B cells consensus epitopes from Glycoprotein E from serotype IV of the dengue virus for exploring new possibilities in vaccine development. The direct implication of the results obtained is to open the way to experimentally validate more epitopes to increase the efficiency of the available treatments against dengue and to explore the methodology in other diseases.
线性b细胞表位的定量预测
在科学文献中,有许多程序可以从蛋白质序列中预测线性b细胞表位。每个程序生成多个可以单独研究的b细胞表位。本文定义了一个函数,该函数结合了有关线性b细胞表位的五种不同预测程序的结果。, BebiPred, EPMLR, BCPred, ABCPred和Emini预测)用于选择最佳b细胞表位。我们从血清型登革热病毒糖蛋白E中获得了17个潜在的线性B细胞一致表位,以探索疫苗开发的新可能性。所获得的结果的直接意义是为实验验证更多的表位开辟了道路,以提高现有治疗登革热的效率,并探索其他疾病的方法。
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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