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Quantitative Prediction of Linear B-Cell Epitopes

机译:线性B细胞表位的定量预测

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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.
机译:在科学文献中,有许多程序可以根据蛋白质序列预测线性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。本文定义了一个称为的函数,该函数结合了五个有关线性B细胞表位的预测程序的结果(即BebiPred,EPLMR,BCPred,ABCPred和Emini Prediction),以选择最佳的B细胞表位。我们从登革病毒血清型IV的糖蛋白E中获得了17个潜在的线性B细胞共有表位,以探索疫苗开发的新可能性。获得的结果的直接含义是为实验验证更多的表位开辟道路,以提高针对登革热的可用治疗的效率,并探索其他疾病的方法。

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