Andzhaparidze O G, Bogomolova N N, Koptiaeva I B, Boriskin Iu S, Chaplygina N M
Vopr Virusol. 1986 Jul-Aug;31(4):430-5.
Synthesis of measles virus proteins in primary and chronic infection of L-41 and HEP-2 cells was studied by radioimmunoprecipitation test and polyacrylamide gel electrophoresis. Synthesis of measles virus main structural proteins, H, P, NP, and M, was found to occur in chronically infected cells. Persistence of measles virus in the systems under study was shown not to be accompanied by changes in electrophoretic mobility of virus polypeptides as compared with proteins synthesized in primary infection. NP protein of the original virus, however, differed significantly from NP protein of the persisting virus in its charge which indicated aminoacid replacements apparently due to mutations of the appropriate region of the virus genome. The mechanism of measles virus persistence in these systems was shown not to be associated with disorders in matrix protein synthesis. Use of monoclonal antibodies in fluorescent antibody technique and radioimmunoprecipitation revealed the stability of a number of antigenic determinants in persisting measles virus in L-41 and HEP-2 cell cultures.
通过放射免疫沉淀试验和聚丙烯酰胺凝胶电泳研究了麻疹病毒蛋白在L - 41和HEP - 2细胞原代感染和慢性感染中的合成情况。发现麻疹病毒主要结构蛋白H、P、NP和M在慢性感染细胞中合成。研究表明,与原代感染中合成的蛋白质相比,所研究系统中麻疹病毒的持续存在并未伴随着病毒多肽电泳迁移率的变化。然而,原始病毒的NP蛋白与其电荷明显不同,这表明氨基酸替代显然是由于病毒基因组相应区域的突变所致。结果表明,这些系统中麻疹病毒持续存在的机制与基质蛋白合成紊乱无关。在荧光抗体技术和放射免疫沉淀中使用单克隆抗体揭示了L - 41和HEP - 2细胞培养物中持续存在的麻疹病毒中许多抗原决定簇的稳定性。