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对产生病毒的小鼠及其他哺乳动物细胞系表面RNA肿瘤病毒主要糖蛋白gp71表达的免疫荧光分析。

Immunofluorescent analysis of expression of the RNA tumor virus major glycoprotein, gp71, on surfaces of virus-producing murine and other mammalian species cell lines.

作者信息

Cloyd M W, Bolognesi D P, Bigner D D

出版信息

Cancer Res. 1977 Mar;37(3):922-30.

PMID:65219
Abstract

The specificity of a single rabbit antiserum pool raised against the purified major glycoprotein, gp71, of Friend murine leukemia virus was determined for a variety of virus-producing mouse, feline, and gibbon ape cell lines by viable cell membrane immunofluorescence absorption. Among murine cells examined, Friend gp71 type specificity was shared only with Rauscher virus-producing cells, and a group specificity was present for all the murine leukemia virus-producing cells tested. Friend and Rauscher murine leukemia virus-infected cells shared interspecies cross-reactivity with feline leukemia and gibbon ape lymphoma virus-producing cells. However, Moloney, Gross, and other virus-producing murine cells shared some, but not all, of these gp71 interspecies determinants with the feline and primate cells. Immunoferritin electron microscopy localized these gp71 antigenic determinants on both virus and cell membranes.

摘要

通过活细胞膜免疫荧光吸收法,针对多种产生病毒的小鼠、猫和长臂猿猿细胞系,测定了用纯化的弗氏小鼠白血病病毒主要糖蛋白gp71免疫制备的单兔抗血清池的特异性。在所检测的鼠细胞中,弗氏gp71型特异性仅与产生劳氏病毒的细胞共有,并且对于所有测试的产生鼠白血病病毒的细胞存在组特异性。感染弗氏和劳氏鼠白血病病毒的细胞与产生猫白血病和长臂猿猿淋巴瘤病毒的细胞具有种间交叉反应性。然而,莫洛尼、格罗斯和其他产生病毒的鼠细胞与猫和灵长类细胞共享了部分但并非全部这些gp71种间决定簇。免疫铁蛋白电子显微镜将这些gp71抗原决定簇定位在病毒和细胞膜上。

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