Sheppard M, Evans L, May J T
Virus Res. 1985 Oct;3(3):287-92. doi: 10.1016/0168-1702(85)90052-8.
By the use of an SV40 origin of replication plasmid vector and the COS-1 cell system, expression of the gene encoding the herpes simplex virus type-2 (HSV-2) major DNA binding protein (ICP8) has been achieved. The HSV-2 4.5 kb BglII 0 DNA fragment containing the ICP8 coding region was inserted into the plasmid vector pSVOd containing the SV40 origin of replication. Transfection of COS-1 cells by the resultant recombinant plasmid (pSVOd20), and subsequent multiplication of this plasmid, led to the production of the HSV-2 major DNA binding protein in sufficient quantities to allow its detection with either monoclonal or polyclonal antibodies as well as sera taken from HSV-2 patients.
通过使用含有SV40复制起点的质粒载体和COS - 1细胞系统,已实现编码单纯疱疹病毒2型(HSV - 2)主要DNA结合蛋白(ICP8)的基因的表达。将含有ICP8编码区的HSV - 2 4.5 kb BglII 0 DNA片段插入到含有SV40复制起点的质粒载体pSVOd中。用所得重组质粒(pSVOd20)转染COS - 1细胞,随后该质粒的增殖,导致产生足够量的HSV - 2主要DNA结合蛋白,从而能够用单克隆或多克隆抗体以及取自HSV - 2患者的血清进行检测。