Schneider J, Schwarz H, Hunsmann G
J Virol. 1979 Feb;29(2):624-32. doi: 10.1128/JVI.29.2.624-632.1979.
Rosette-shaped particles mainly containing gp85 were isolated from Friend leukemia virus. The isolation procedure comprised lysis of the virion by Triton X-100, affinity chromatography on concanavalin A-Sepharose, and velocity sedimentation. The rosettes displayed a mean sedimentation constant of 32S and a buoyant density of 1.21 g/ml. They contained 1% Triton X-100 and about 2% phospholipid. gp85 was identified by polyacrylamide electrophoresis, staining with periodic acid-Schiff reagent, and immunoprecipitation with antisera against Friend leukemia virus gp71 and p15(E). Rosettes completely blocked the cytotoxicity of the gp71 antiserum. The ability to hemagglutinate was inhibited by antibodies to gp71.
从弗氏白血病病毒中分离出主要含gp85的玫瑰花结状颗粒。分离步骤包括用Triton X-100裂解病毒体、在伴刀豆球蛋白A-琼脂糖上进行亲和层析以及速度沉降。这些玫瑰花结显示平均沉降常数为32S,浮力密度为1.21 g/ml。它们含有1%的Triton X-100和约2%的磷脂。通过聚丙烯酰胺电泳、用高碘酸-希夫试剂染色以及用抗弗氏白血病病毒gp71和p15(E)的抗血清进行免疫沉淀来鉴定gp85。玫瑰花结完全阻断了gp71抗血清的细胞毒性。血凝能力受到抗gp71抗体的抑制。