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Identification of immunodominant VP1 linear epitope of enterovirus71 (EV71) using synthetic peptides for detecting human anti-EV71 IgG antibodies in western blots

机译:使用合成肽在Western印迹中检测人抗-EV71 IgG抗体,鉴定肠道病毒71(EV71)的免疫显性Vp1线性表位

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摘要

A major IgG-specific immunodominant VP1 linear epitope of enterovirus 71 (EV71) strain 41 (5865/SIN/00009), defined by the core sequence LEGTTNPNG, was identified by Pepscan analysis. Oligonucleotides corresponding to the amino-acid sequence of synthetic peptide SP32 were cloned and over-expressed in Escherichia coli as a recombinant glutathione-S-transferase (GST)-SP32 fusion protein. In ELISAs, this protein did not react with human anti-EV71 IgG antibodies, but there was significant immunoreactivity according to western blot analysis. The amino-acid sequence of SP32 was highly specific for detecting EV71 strains in western blot analysis, and showed no immunoreactivity with monoclonal antibodies raised against other enteroviruses, e.g., CA9 and Echo 6.
机译:肠病毒71(EV71)41株(5865 / SIN / 00009)的主要IgG特异性免疫优势VP1线性表位,由核心序列LEGTTNPNG定义,通过Pepscan分析鉴定。克隆了对应于合成肽SP32氨基酸序列的寡核苷酸,并将其作为重组谷胱甘肽-S-转移酶(GST)-SP32融合蛋白在大肠杆菌中过表达。在ELISA中,该蛋白不与人抗EV71 IgG抗体反应,但是根据Western blot分析,该蛋白具有显着的免疫反应性。 SP32的氨基酸序列对Western印迹分析中的EV71菌株检测具有高度特异性,并且与针对其他肠病毒(例如CA9和Echo 6)的单克隆抗体没有免疫反应。

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