Takeda N, Yang C F, Kuhn R J, Wimmer E
Department of Microbiology, School of Medicine, State University of New York, Stony Brook 11794.
Virus Res. 1987 Sep;8(3):193-204. doi: 10.1016/0168-1702(87)90015-3.
The properties of an in vitro replication system derived from a membrane fraction (crude replication complex, CRC) of poliovirus-infected HeLa cells were examined. This system was capable of producing the nucleotidyl-proteins VPg-pU and VPg-pUpU. Due to high intrinsic phosphoesterase(s) activity and endogenous nucleoside triphosphate pools the yield of labeled product was low. Treatment of CRC with DEAE-cellulose and addition of an ATP generating system resulted in a dramatic increase in the level of nucleotidyl-proteins formed. The capacity to form VPg-pU and VPg-pUpU could be completely abolished by pretreatment of CRC with nuclease, an observation suggesting that the uridylylation of VPg is a template-dependent reaction.
对源自脊髓灰质炎病毒感染的HeLa细胞膜组分(粗制复制复合物,CRC)的体外复制系统的特性进行了研究。该系统能够产生核苷酸蛋白VPg-pU和VPg-pUpU。由于高内在磷酸酯酶活性和内源性核苷三磷酸池,标记产物的产量较低。用DEAE-纤维素处理CRC并添加ATP生成系统导致形成的核苷酸蛋白水平显著增加。用核酸酶预处理CRC可完全消除形成VPg-pU和VPg-pUpU的能力,这一观察结果表明VPg的尿苷酸化是一种模板依赖性反应。