恶性疟原虫MSP-1和EBA-140肽与HLA II类肽结合的预测

Javier Rodríguez, Pedro Bernal, Luisa Álvarez, Sandra Pabón, Sandra Ibáñez, Nanyid Chapuel, Héctor Pérez, Alexandra Correa, Luis Carlos Salazar, Raúl Walteros
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引用次数: 15

摘要

MSP-1 merozoite表面蛋白与疟疾对红细胞的侵袭现象有关,EBA-140抗原蛋白与红细胞表面的唾液糖蛋白相互作用。从两种结合HLA II类的蛋白中鉴定肽对疫苗的开发具有特别重要的意义。在本工作中,基于熵的S/k比例,应用预测HLA II类结合理论,预测了蛋白MSP-1和EBA-140对这两个分子的20个氨基酸序列的结合现象。分别计算了948个和732个MSP-1和EBA-140的非线性重叠序列的概率值、组合值和熵值。计算构建了三个长度为500个氨基酸的理论蛋白质,以便将开发的结合理论应用于所有的非聚合物重叠肽。结果表明,所研究的两种分裂子蛋白中,有298个序列与结合大状态有关,1409个序列与非结合大状态有关。所建立的理论预测有助于疫苗开发过程中多肽的选择。对于构建的3个理论蛋白,预测第111、84和72序列包含在结合大状态中,而序列381、408和420序列被预测为与非结合大状态相关。这些预测是抗原呈递的物理和数学顺序的证据,这可能对疫苗的开发有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predicción de unión de péptidos de MSP-1 y EBA-140 de Plasmodium falciparum al HLA clase II

The MSP-1 merozoite surface protein is related to the invasion phenomenon of malaria to red cells, while the EBA-140 antigen protein interacts with the sialoglycoproteins on the surface of erythrocytes. The identification of peptides from both proteins that bind to HLA class II has a particular importance for the development of vaccines.

In the present work, a predictive binding to HLA class II theory, based on S/k proportion of entropy was applied, for the prediction of proteins MSP-1 and EBA-140 binding phenomenon to the totality of 20 amino acid sequences of both molecules. The probability, combinatory and entropy values were calculated for 948 and 732 nonamer overlapping sequences of MSP-1 and EBA-140, respectively. Three theoretical proteins of 500 aminoacids of lenght each were computationally built in order to apply the developed binding theory to all their nonamer overlapping peptides.

It was predicted that for the two studied merozoite proteins, 298 sequences are related to the binding macrostate and 1409 to the not-binding macrostate. The developed theoretical prediction can facilitate the selection of peptides during the process of vaccine development. For the three theoretical proteins built, it was found that 111, 84 and 72 are predicted as included into the binding macrostate, while sequences 381, 408, and 420 are predicted as related to the not-binding macrostate.

The predictions are an evidence of a physical and mathematical order in antigen presentation, which can be useful to the development of vaccines.

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