Wolff L, Koller R, Ruscetti S
J Virol. 1982 Aug;43(2):472-81. doi: 10.1128/JVI.43.2.472-481.1982.
Monoclonal antibodies which recognize a region common to Friend spleen focus-forming virus encoded gp52 and Friend mink cell focus-inducing viral gp70 were isolated. One such antibody from hybridoma 7C10 was tested extensively in immune precipitation and was found to react with a determinant on envelope gp70s of all mink cell focus-inducing, xenotropic, and amphotropic mouse retroviruses tested, but not with envelope gp70s of ecotropic viruses, including Friend, Moloney, and AKR murine leukemia viruses. Monoclonal antibody from hybridoma 7C10 precipitated a 23,000-molecular-weight fragment, derived by V8 protease digestion of Friend mink cell focus-inducing gp70. This 23,000-molecular-weight peptide was determined to derive from the amino terminus of the molecule. These results correlate well with other genetic data which indicate that endogenously acquired sequences of mink cell focus-inducing viruses are found at the 5' end of the envelope gene.
分离出了能识别弗氏脾脏灶形成病毒编码的gp52和弗氏貂细胞灶诱导病毒gp70共同区域的单克隆抗体。对来自杂交瘤7C10的一种此类抗体进行了广泛的免疫沉淀测试,发现它能与所有测试的貂细胞灶诱导、嗜异性和双嗜性小鼠逆转录病毒包膜gp70上的一个决定簇发生反应,但不与亲嗜性病毒的包膜gp70发生反应,这些亲嗜性病毒包括弗氏、莫洛尼和AKR鼠白血病病毒。来自杂交瘤7C10的单克隆抗体沉淀出一个23000分子量的片段,该片段是通过对弗氏貂细胞灶诱导gp70进行V8蛋白酶消化得到的。这个23000分子量的肽被确定来自该分子的氨基末端。这些结果与其他遗传数据高度相关,这些遗传数据表明,在包膜基因的5'端发现了貂细胞灶诱导病毒的内源性获得序列。