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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Mapping of linear epitopes on fibre knob of human adenovirus serotype 5.
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Mapping of linear epitopes on fibre knob of human adenovirus serotype 5.

机译:线性表位在人腺病毒血清型5的纤维瘤上的定位

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摘要

Linear antigenic epitopes on the Ad5 fibre knob (FK5) were characterised with fibre- and virion-specific antisera, using 15-mer overlapping peptides covering the knob of the fibre. They were compared with epitopes on the Ad2 fibre knob (FK2) domain. The stronger reactive FK5 epitopes were represented by peptides P3 (amino acids (aa A419-L433)), P6 (aa S449-E463), P7 (aa I459-L473), P12 (aa G509-N523), P14 (aa P529-G543) and P16 (aa A549-Y563). P3 spans the B beta-strand and the left portion of the C beta-strand, P6 and P7 the D beta-strand and the adjacent parts of the CD and DE loops, P12, P14 and P16 the G, H and I beta strands and the adjacent parts of the loops, respectively. The stronger reactive epitopes on FK2 were located in P2 (aa P409-L423), P6 (aa T449-Q463), P8 (aa E469-G483), P13 (aa Q519-T533) and P16 (aa S549-K563). The positions of FK5 and FK2 derived peptides, representing epitopes, are either identical or overlapping or adjacent, as determined by amino acid sequence alignment. Antisera obtained against several longer peptides showed virus neutralising capacity, indicating neutralising epitopes in these peptides.
机译:Ad15纤维纽结(FK5)上的线性抗原表位通过覆盖纤维纽结的15-mer重叠肽,以纤维和病毒体特异性抗血清为特征。将它们与Ad2纤维结(FK2)域上的表位进行比较。较强的反应性FK5表位由肽P3(氨基酸(aa A419-L433)),P6(aa S449-E463),P7(aa I459-L473),P12(aa G509-N523),P14(aa P529- G543)和P16(aa A549-Y563)。 P3跨越Bβ链,Cβ链的左侧,P6和P7跨越Dβ链,CD和DE环的相邻部分,P12,P14和P16跨越G,H和Iβ链。和循环的相邻部分。 FK2上较强的反应性表位位于P2(aa P409-L423),P6(aa T449-Q463),P8(aa E469-G483),P13(aa Q519-T533)和P16(aa S549-K563)。通过氨基酸序列比对确定,代表表位的FK5和FK2衍生肽的位置相同或重叠或相邻。针对几种更长的肽获得的抗血清显示出病毒中和能力,表明这些肽中和了表位。

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