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利用大肠杆菌表达系统对禽轮状病毒主要内衣壳蛋白上的抗原位点进行定位。

Mapping of antigenic sites on the major inner capsid protein of avian rotavirus using an Escherichia coli expression system.

作者信息

Ito H, Minamoto N, Goto H, Luo T R, Sugiyama M, Kinjo T

机构信息

Department of Veterinary Public Health, Faculty of Agriculture, Gifu University, Japan.

出版信息

Arch Virol. 1996;141(11):2129-38. doi: 10.1007/BF01718220.

Abstract

The cDNA encoding the VP6 gene of avian rotavirus PO-13 strain was inserted into the bacterial expression vector pET-3a. Upon isopropyl-1-thio-beta-D-galactoside induction, the E. coli BL21 (DE3) harboring the vector containing cDNA of the VP6 gene produced an approximately 45-kDa polypeptide, which reacted with rabbit serum against PO-13 strain in Western blotting. To study the antigenic sites on VP6, various deletion mutants were constructed, expressed in E. coli and the reactivity with antigenic site I- and II-specific MAbs analyzed by Western blotting. Site I, which is shared with all group A mammalian and avian rotaviruses except for chicken rotavirus, was found to be located at amino acid positions 45 to 65, and site II, which probably contributes to an authentic group A antigen common to both mammalian and avian rotaviruses, at amino acid positions 134 to 142.

摘要

将编码禽轮状病毒PO - 13株VP6基因的cDNA插入细菌表达载体pET - 3a。经异丙基 - 1 - 硫代 - β - D - 半乳糖苷诱导后,携带含有VP6基因cDNA载体的大肠杆菌BL21(DE3)产生了一条约45 kDa的多肽,该多肽在蛋白质印迹法中与抗PO - 13株的兔血清发生反应。为了研究VP6上的抗原位点,构建了各种缺失突变体,在大肠杆菌中表达,并通过蛋白质印迹法分析其与抗原位点I和II特异性单克隆抗体的反应性。发现位点I位于氨基酸位置45至65,所有A组哺乳动物和禽轮状病毒(除鸡轮状病毒外)都共有该位点;位点II位于氨基酸位置134至142,它可能是哺乳动物和禽轮状病毒共有的真正A组抗原的组成部分。

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