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Antigenic epitopes of viral polyprotein: an approachfor fragment based peptide vaccines from PapayaRingspot virus

机译:病毒多蛋白抗原表位:木瓜环斑病毒基于片段的肽疫苗的方法

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Papaya ringspot is a destructive disease characterized by a yellowing and stunting of the crown of papaya trees and assay was designed to help assign putative genome polyprotein analysis of Papaya ringspot virus strain W. We used different methods for the prediction of linear epitopes using a combination of a hidden Markov model and a propensity scale method. Data set was collected from the literature, and data sets of epitopes in the genome polyprotein having twenty four antigenic determinants in 675 residues long sequence. The structural homology modeling method is allows potential drug targets to identify active sites i.e. linear epitopes, which form antibodies in host cells. The method integrates prediction of peptide MHC class I binding; proteasomal C terminal cleavage and TAP transport efficiency. The challenges for the future are to establish the function of all of protein structures. In this assay we use of multiple methods towards the accurate identification of antigenic epitopes. The proposed approach is useful not only for plant and viral biology but it covers the wide area of vaccines and antibodies for therapeutic purposes in humans.
机译:木瓜环斑是一种破坏性疾病,其特征是木瓜树冠发黄和发育迟缓,其检测方法旨在帮助对木瓜环斑病毒株W进行推定的基因组多蛋白分析。我们使用了多种方法来预测线性表位,结合使用隐藏的马尔可夫模型和倾向量表方法。从文献中收集数据集,并且在675个残基长序列中具有二十四个抗原决定簇的基因组多蛋白中的表位的数据集。结构同源性建模方法允许潜在的药物靶标鉴定活性位点,即线性表位,其在宿主细胞中形成抗体。该方法整合了对肽类MHC I类结合的预测;蛋白酶体C末端裂解和TAP运输效率。未来的挑战是建立所有蛋白质结构的功能。在该测定中,我们使用多种方法来准确鉴定抗原表位。所提出的方法不仅对植物和病毒生物学有用,而且涵盖了用于人类治疗目的的疫苗和抗体的广泛领域。

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