Processing of envelope polypeptides of herpes simplex virus type 1. Demonstration of variation in different cell lines by high-performance liquid chromatography and radioimmunoprecipitation.

Journal of chromatography Pub Date : 1994-02-11
G Kessie, D M Dela Cruz, M A Taha, F J al-Shammary, A F Tawfik, M N al-Ahdal
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引用次数: 0

Abstract

[35S]Methionine-labelled envelope polypeptides of herpes simplex virus type 1, strain F, propagated in mammalian cell culture of various origins, were separated by ion-exchange high-performance liquid chromatography on a TSK DEAE-3SW column. Analysis of the fractions by radioimmunoprecipitation followed by sodium dodecyl sulphate polyacrylamide gel electrophoresis of the immunoprecipitates showed similarities as well as distinct differences in the number, migration patterns and molecular mass of the synthesized polypeptides, depending on the host cell. The results show that this method can be used to demonstrate species-specific or organ-specific differences in the processing of virus-specified polypeptides synthesized in host cells.

1型单纯疱疹病毒包膜多肽的处理。用高效液相色谱法和放射免疫沉淀法证明不同细胞系的差异。
[35]在TSK DEAE-3SW柱上,用离子交换高效液相色谱分离了在不同来源的哺乳动物细胞培养中繁殖的1型单纯疱疹病毒F株的蛋氨酸标记包膜多肽。用放射免疫沉淀法和十二烷基硫酸钠聚丙烯酰胺凝胶电泳对免疫沉淀物进行分析,结果表明,不同宿主细胞合成的多肽在数量、迁移模式和分子质量上既有相似之处,也有明显差异。结果表明,该方法可用于证明宿主细胞合成的病毒特异性多肽加工过程中的物种特异性或器官特异性差异。
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