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Weighted lambda superstrings applied to vaccine design

机译:加权λ超弦应用于疫苗设计

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摘要

We generalize the notion of λ-superstrings, presented in a previous paper, to the notion of weighted λ-superstrings. This generalization entails an important improvement in the applications to vaccine designs, as it allows epitopes to be weighted by their immunogenicities. Motivated by these potential applications of constructing short weighted λ-superstrings to vaccine design, we approach this problem in two ways. First, we formalize the problem as a combinatorial optimization problem (in fact, as two polynomially equivalent problems) and develop an integer programming (IP) formulation for solving it optimally. Second, we describe a model that also takes into account good pairwise alignments of the obtained superstring with the input strings, and present a genetic algorithm that solves the problem approximately. We apply both algorithms to a set of 169 strings corresponding to the Nef protein taken from patiens infected with HIV-1. In the IP-based algorithm, we take the epitopes and the estimation of the immunogenicities from databases of experimental epitopes. In the genetic algorithm we take as candidate epitopes all 9-mers present in the 169 strings and estimate their immunogenicities using a public bioinformatics tool. Finally, we used several bioinformatic tools to evaluate the properties of the candidates generated by our method, which indicated that we can score high immunogenic λ-superstrings that at the same time present similar conformations to the Nef virus proteins.
机译:我们将先前论文中介绍的λ超弦的概念推广到加权λ超弦的概念。这种概括需要在疫苗设计应用中进行重大改进,因为它可以通过其免疫原性来加权表位。由于在疫苗设计中构建短加权λ超弦的这些潜在应用的动机,我们以两种方式解决此问题。首先,我们将该问题形式化为组合优化问题(实际上,作为两个多项式等价问题),并开发一种整数编程(IP)公式来优化求解。其次,我们描述了一个模型,该模型还考虑了所获得的超级字符串与输入字符串的良好成对对齐,并提出了一种遗传算法来近似解决该问题。我们将这两种算法应用于与从感染了HIV-1的患者身上获得的Nef蛋白相对应的169个字符串中。在基于IP的算法中,我们从实验性抗原决定簇的数据库中获取抗原决定簇和免疫原性的估计。在遗传算法中,我们将169个字符串中存在的所有9-mer作为候选表位,并使用公共生物信息学工具估算其免疫原性。最后,我们使用了多种生物信息学工具来评估通过我们的方法生成的候选基因的特性,这表明我们可以对高免疫原性的λ超弦评分,同时呈现与Nef病毒蛋白相似的构象。

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