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In silico epitope (T-228) rabies virus vaccine.

机译:在硅片表位(t - 228)狂犬病毒疫苗。

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摘要

Accession FJ979833 was used to extract human epitopes from rabies virus glycoprotein database. Strongest binders with MHC molecules were determined by artificial neural network and stabilized matrix methods with highest scores subjected to clustal W alignment for conservancy. An epitope from position 228-236 (T-228) was identified as a novel T cell epitope revealing good MHC class I binding, processing and conservation in known rabies viruses. The findings suggest that it may be possible to generatea synthetic peptide vaccine against rabies but further research on G protein is required, including a search for additional linear epitopes.
机译:加入FJ979833被用来提取人类从数据库狂犬病毒糖蛋白抗原表位。最强的绑定与MHC分子由人工神经网络和决定稳定矩阵方法得分最高为保护受到clustal W对齐。位置的抗原决定基228 - 236 (t - 228)确认为小说T细胞表位暴露MHC类我绑定好,加工在已知的狂犬病病毒保护。研究结果表明,它可能会generatea合成肽疫苗狂犬病,但对G蛋白的进一步研究要求,包括寻找额外的线性抗原表位。

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