Greenfield R S, Kiener P A, Chin D P, Curry R C, Spitalny G L
J Leukoc Biol. 1986 Dec;40(6):665-76. doi: 10.1002/jlb.40.6.665.
A rapid one-step procedure for the purification of natural murine gamma interferon (MuIFN-gamma) by immunoaffinity chromatography has been developed. Crude MuIFN-gamma was passed through a column containing immobilized anti-MuIFN-gamma monoclonal antibody, and the column was washed with high salt and detergent. Active MuIFN-gamma was subsequently eluted with ammonium thiocyanate/glycerol (yields of 20-40%). Analysis of the immunopurified interferon by sodium dodecyl sulfate polyacrylamide gel electrophoresis under reducing conditions revealed biologically active bands of about 19.5, and 14 kd. Under nonreducing conditions, three active bands at 35, 19.5, and 14 kd could be seen. Gel filtration of the immunopurified MuIFN-gamma under reducing or nonreducing conditions showed a single major peak of antiviral activity corresponding to a molecular weight of 43 kd. The protein eluted from each band from the SDS-gel, in addition to possessing antiviral activity, was shown to activate macrophages in three assays: macrophage tumoricidal activity, hydrogen peroxide secretion, and expression of la antigen on the surface of exudate macrophages.
已开发出一种通过免疫亲和色谱法快速一步纯化天然鼠γ干扰素(MuIFN-γ)的方法。将粗制的MuIFN-γ通过含有固定化抗MuIFN-γ单克隆抗体的柱,并用高盐和去污剂洗涤该柱。随后用硫氰酸铵/甘油洗脱活性MuIFN-γ(产率为20-40%)。在还原条件下通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳对免疫纯化的干扰素进行分析,显示出约19.5和14kd的生物活性条带。在非还原条件下,可以看到35、19.5和14kd的三条活性条带。在还原或非还原条件下对免疫纯化的MuIFN-γ进行凝胶过滤,显示出一个单一的主要抗病毒活性峰,对应分子量为43kd。从SDS凝胶的每个条带洗脱的蛋白质,除了具有抗病毒活性外,在三种测定中还显示出激活巨噬细胞的作用:巨噬细胞杀肿瘤活性、过氧化氢分泌以及渗出液巨噬细胞表面Ia抗原的表达。