Horowitz S A, Garrett B, Davis J K, Cassell G H
Infect Immun. 1987 May;55(5):1314-20. doi: 10.1128/iai.55.5.1314-1320.1987.
Labeling of Mycoplasma pulmonis cells by iodination with the Bolton-Hunter reagent was shown to efficiently label membrane-associated proteins without significant loss of viability. Labeled proteins proven to be surface exposed by differential proteolytic digestion were analyzed by autoradiography of two-dimensional polyacrylamide gel electrophoresis (PAGE), and seven labeled major polypeptides were identified. To identify all the membrane-associated antigens, pure membranes were isolated by using the surface-labeled proteins as markers. Analysis of the isolated membranes by autoradiography of both sodium dodecyl sulfate-PAGE and the two-dimensional PAGE indicated that the labeled surface proteins were retained in the pure membranes; by immunoblotting with sera from naturally infected animals, these surface proteins were shown to be the predominant antigens recognized by the host during natural infection.
用博尔顿 - 亨特试剂碘化法对肺炎支原体细胞进行标记,结果表明该方法能有效标记膜相关蛋白,且细胞活力无显著损失。通过二维聚丙烯酰胺凝胶电泳(PAGE)放射自显影分析经差异蛋白酶消化证明为表面暴露的标记蛋白,鉴定出了7种标记的主要多肽。为鉴定所有膜相关抗原,以表面标记蛋白为标志物分离出纯膜。通过十二烷基硫酸钠 - PAGE和二维PAGE放射自显影对分离出的膜进行分析,结果表明标记的表面蛋白保留在纯膜中;用自然感染动物的血清进行免疫印迹分析显示,这些表面蛋白是宿主在自然感染期间识别的主要抗原。