Lanford R E
Department of Virology and Immunology, Southwest Foundation for Biomedical Research, San Antonio, Texas 78284.
Virology. 1988 Nov;167(1):72-81. doi: 10.1016/0042-6822(88)90055-4.
Simian virus 40 (SV40) large T and small t antigens were synthesized in insect cells using the baculovirus Autographa californica as an expression vector. A recombinant virus containing a genomic copy of the SV40 early region expressed high levels of small t antigen but only low levels of large T antigen. However, very high levels of T antigen synthesis were observed when viruses were constructed with a cDNA copy of the large T antigen mRNA. Insect cells were capable of modifying T antigen by phosphorylation, palmitylation, glycosylation, and oligomerization. Functional assays demonstrated that the origin-specific DNA binding, ATPase, and helicase activities of insect cell-derived T antigen were comparable to T antigen synthesized in mammalian cells. Use of the baculovirus vector system to produce T antigen should facilitate future investigations requiring large quantities of T antigen.
使用苜蓿银纹夜蛾核型多角体病毒作为表达载体,在昆虫细胞中合成了猴病毒40(SV40)大T抗原和小t抗原。含有SV40早期区域基因组拷贝的重组病毒表达高水平的小t抗原,但仅表达低水平的大T抗原。然而,当用大T抗原mRNA的cDNA拷贝构建病毒时,观察到非常高水平的T抗原合成。昆虫细胞能够通过磷酸化、棕榈酰化、糖基化和寡聚化修饰T抗原。功能分析表明,昆虫细胞来源的T抗原的起始特异性DNA结合、ATP酶和解旋酶活性与在哺乳动物细胞中合成的T抗原相当。使用杆状病毒载体系统生产T抗原应有助于未来需要大量T抗原的研究。