Fischinger P J, Lange J, Schäfer W
Proc Natl Acad Sci U S A. 1972 Jul;69(7):1900-4. doi: 10.1073/pnas.69.7.1900.
A highly purified gel electrophoretic fraction of murine leukemia virus (MuLV) can confer enhanced infectivity on MuLV derived from tissue culture and can protect MuLV from neutralization by specific antiserum. Of the known viral proteins tested, a purified electrophoretic fraction (14,000 daltons) is the only active fraction and seems to consist of the group-specific antigen I and an associated lipid moiety. The action of this fraction obtained from one type of MuLV is group-specific in that it can enhance and protect serologically different types of MuLV. The effect of this fraction is exerted on viruses and not on cells. MuLV derived from tumors was not enhanced by the fraction, but became amenable to its action after a single passage through tissue culture. Reconstruction experiments suggested that the fraction may consist of an exterior protein associated with some lipids. This complex, which apparently protrudes on the viral surface, is required for infectivity and shields the type-specific antigen containing the hemagglutinating site.
高度纯化的鼠白血病病毒(MuLV)凝胶电泳组分可增强源自组织培养的MuLV的感染性,并能保护MuLV不被特异性抗血清中和。在所测试的已知病毒蛋白中,一种纯化的电泳组分(14000道尔顿)是唯一的活性组分,似乎由群特异性抗原I和一个相关的脂质部分组成。从一种类型的MuLV获得的该组分的作用具有群特异性,因为它可以增强和保护血清学上不同类型的MuLV。该组分的作用是作用于病毒而非细胞。源自肿瘤的MuLV不会被该组分增强,但在通过组织培养单次传代后变得对其作用敏感。重建实验表明,该组分可能由与一些脂质相关的外部蛋白组成。这种复合物显然突出于病毒表面,对于感染性是必需的,并屏蔽了含有血凝位点的型特异性抗原。