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A Database for Prediction of Unique Peptide Motifs as Linear Epitopes

机译:预测独特肽基作为线性表位的数据库

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A linear epitope prediction database (LEPD) is designed for identification of unique peptide motifs (UPMs) as specific linear epitopes for all protein families defined by Pfam. The UPMs in LEPD are extracted from each protein family by employing reinforced merging techniques that merge the primary unique patterns into a consecutive peptide based on the neighboring relationships and various levels of parameter settings. These merged peptide motifs are examined using the physicochemical and structural propensity scales for antigenic characteristics and are verified by employing background model analysis for specificity. The filtered UPMs with high antigenicity and specificity are considered as linear epitopes that provide important information for designing antibodies and vaccines. The predicted epitopes of each protein family in the LEPD can be searched in a straightforward manner, and the corresponding chemical properties be displayed in graphical and tabular formats. To verify the specificity of the predicted epitopes, each identified UPM is analyzed by scanning over the complete genomes of a series of model organisms. For any query protein possessing a resolved 3D structure, the proposed database also provides interactive visualization of the protein structures for allocation and comparison of the predicted linear epitopes. The accuracy of the prediction algorithm is evaluated to be higher than 70% in terms of mapping a UPM as a linear epitope as compared to the known databases.
机译:线性表位预测数据库(LEPD)设计用于鉴定独特的肽基序(UPM),作为Pfam定义的所有蛋白质家族的特定线性表位。 LEPD中的UPM通过采用增强的合并技术从每个蛋白质家族中提取,该合并技术基于相邻关系和各种级别的参数设置将主要的独特模式合并为连续的肽。使用理化和结构倾向量表检查这些合并的肽基序是否具有抗原特性,并通过采用背景模型分析来验证其特异性。具有高抗原性和特异性的过滤后的UPM被认为是线性表位,可为设计抗体和疫苗提供重要信息。可以直接搜索LEPD中每个蛋白质家族的预测表位,并以图形和表格形式显示相应的化学性质。为了验证预测表位的特异性,通过扫描一系列模型生物的完整基因组来分析每个鉴定出的UPM。对于具有解析的3D结构的任何查询蛋白,建议的数据库还提供了蛋白结构的交互可视化,以分配和比较预测的线性表位。与将UPM映射为线性表位相比,预测算法的准确性被评估为高于70%。

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