Alexander D J, Collins M S
Microbios. 1977;18(72):87-98.
Purification of egg-grown infectious bronchitis virus (IBV) by sucrose density gradient centrifugation alone, or sucrose density gradient centrifugation plus pH 8.0 treatment, concanavalin A precipitation or metrizamide density gradient centrifugation, failed to produce any differences in the virus polypeptide pattern following polyacrylamide gel electrophoresis in the presence of SDS(SDS-PAGE). SDS-PAGE of purified IBV on 7.5% acrylamide gels separated 16 polypeptides which were detectable by staining with Coomassie blue or measurement of radioactivity following electrophoresis of (3H)-leucine labelled IBV. The molecular weights of the polypeptides were within the range 15,000-135,000. The polypeptides of egg and chick kidney (CK) cell-grown IBV were identical in both size and number but quantitative differences were detected. In particular the relative proportion of the major 52,000 molecular weight polypeptide was greatly reduced in IBV grown in CK cells. SDS-PAGE of purified IBV and staining with Schiff's reagent to detect carbohydrate revealed four.bands with molecular weights of 128,000, 86,000, 67,500 and 37,000. The 128,000 band did not correspond to any of the detected polypeptides. Use of 5% acrylamide gels for SDS-PAGE of IBV failed to resolve all the minor polypeptides and only seven bands were detected.
仅通过蔗糖密度梯度离心法,或蔗糖密度梯度离心法加pH 8.0处理、伴刀豆球蛋白A沉淀法或甲泛葡胺密度梯度离心法来纯化鸡胚培养的传染性支气管炎病毒(IBV),在十二烷基硫酸钠存在下进行聚丙烯酰胺凝胶电泳(SDS-PAGE)后,病毒多肽图谱未产生任何差异。在7.5%丙烯酰胺凝胶上对纯化的IBV进行SDS-PAGE,分离出16种多肽,这些多肽可通过考马斯亮蓝染色或对(3H)-亮氨酸标记的IBV进行电泳后的放射性测量来检测。这些多肽的分子量在15,000至135,000范围内。鸡胚和鸡肾(CK)细胞培养的IBV多肽在大小和数量上相同,但存在定量差异。特别是在CK细胞中生长的IBV中,主要的52,000分子量多肽的相对比例大大降低。对纯化的IBV进行SDS-PAGE并用席夫试剂染色以检测碳水化合物,发现有四条带,分子量分别为128,000、86,000、67,500和37,000。128,000的条带与任何检测到的多肽均不对应。使用5%丙烯酰胺凝胶对IBV进行SDS-PAGE无法分辨所有次要多肽,仅检测到七条带。