Molitor T W, Joo H S, Collett M S
J Virol. 1985 Sep;55(3):554-9. doi: 10.1128/JVI.55.3.554-559.1985.
Sera from porcine parvovirus (PPV)-infected swine fetuses immunoprecipitated and 84- to 86-kilodalton polypeptide in addition to the A and B virion structural proteins. This polypeptide, designated NS-1, was present in PPV-infected cell lysates but not in purified virions. Partial proteolysis mapping revealed that NS-1 was not related to the A and B viral structural proteins. All three proteins in infected cells were phosphorylated at serine residues, and NS-1 also contained phosphothreonine. From pulse-labeling experiments with either 32Pi or [35S]methionine, NS-1 was found to first appear 5 to 7 h postinfection, whereas the viral structural polypeptides were first synthesized 9 to 11 h postinfection. Pulse-chase experiments revealed that NS-1 initially appeared as an 84-kilodalton protein and was subsequently structurally modified to forms of slower electrophoretic mobilities. The time of appearance of NS-1 after virus infection coincided with the initiation of viral DNA synthesis, suggesting that this polypeptide (and the modified forms thereof) may be involved in PPV replication.
来自感染猪细小病毒(PPV)的猪胎儿的血清除了能免疫沉淀A和B病毒粒子结构蛋白外,还能免疫沉淀84至86千道尔顿的多肽。这种多肽被命名为NS-1,存在于PPV感染的细胞裂解物中,但不存在于纯化的病毒粒子中。部分蛋白酶解图谱分析表明,NS-1与A和B病毒结构蛋白无关。感染细胞中的所有三种蛋白质在丝氨酸残基处都被磷酸化,并且NS-1还含有磷酸苏氨酸。通过用32Pi或[35S]甲硫氨酸进行脉冲标记实验发现,NS-1在感染后5至7小时首次出现,而病毒结构多肽在感染后9至11小时首次合成。脉冲追踪实验表明,NS-1最初以84千道尔顿的蛋白质形式出现,随后在结构上被修饰为电泳迁移率较慢的形式。病毒感染后NS-1出现的时间与病毒DNA合成的起始时间一致,这表明这种多肽(及其修饰形式)可能参与了PPV的复制。