Norrild B, Pedersen B, Roizman B
Infect Immun. 1981 Feb;31(2):660-7. doi: 10.1128/iai.31.2.660-667.1981.
In this paper we report that viral polypeptides from herpes simplex virus 1 (HSV-1) and 2 (HSV-2)-infected cells electrophoretically separated in sodium dodecyl sulfate-polyacrylamide-agarose gels and transferred to diazobenzyloxymethyl paper can react with rabbit hyperimmune sera, both polyvalent and prepared against specific antigens. The polyvalent hyperimmune sera against HSV-1 reacted with 17 HSV-1 polypeptide bands and 8 HSV-2 polypeptide bands. Concordantly, polyvalent sera against HSV-2 reacted with at least 16 HSV-2 polypeptide bands and 8 HSV-1 polypeptide bands. The antisera prepared against the specific antigens reacted with a smaller number of polypeptide bands. Preimmune sera and immune sera did not react with electrophoretically separated polypeptides from infected and uninfected cells, respectively. The immune localization of separated antigens test provides a powerful technique for identification of immunogenic viral polypeptides, especially those which are normally insoluble and therefore unavailable for immunological reactivity in immune precipitation tests.
在本文中,我们报道了从单纯疱疹病毒1型(HSV-1)和2型(HSV-2)感染细胞中提取的病毒多肽,经十二烷基硫酸钠-聚丙烯酰胺-琼脂糖凝胶电泳分离后转移至重氮苄氧基甲基纸上,可与兔超免疫血清发生反应,包括多价血清以及针对特定抗原制备的血清。针对HSV-1的多价超免疫血清与17条HSV-1多肽带和8条HSV-2多肽带发生反应。同样,针对HSV-2的多价血清与至少16条HSV-2多肽带和8条HSV-1多肽带发生反应。针对特定抗原制备的抗血清与较少数量的多肽带发生反应。免疫前血清和免疫血清分别不与来自感染和未感染细胞的经电泳分离的多肽发生反应。分离抗原的免疫定位试验为鉴定免疫原性病毒多肽提供了一种强大的技术,尤其是那些通常不溶性因而在免疫沉淀试验中无法进行免疫反应的多肽。