Frame M C, Purves F C, McGeoch D J, Marsden H S, Leader D P
MRC Virology Unit, Institute of Virology, Glasgow, U.K.
J Gen Virol. 1987 Oct;68 ( Pt 10):2699-704. doi: 10.1099/0022-1317-68-10-2699.
Previous work has shown that a novel protein kinase is induced after infection of cultured cells with herpes simplex virus type 1 (HSV-1). Separately, it has been reported that the protein encoded by HSV-1 gene US3 shows similarity in its amino acid sequence to members of the protein kinase family of eukaryotes. We have investigated the possibility that these two observations are connected by preparing an antiserum to a synthetic oligopeptide corresponding to the carboxy-terminal eight amino acids of the US3 protein. This antiserum reacted on immunoblots with a polypeptide of apparent molecular weight 68,000 from extracts of cells which had been infected with HSV-1. The antiserum also reacted strongly with a 68,000 molecular weight species from a preparation of the novel HSV-1 protein kinase which had been extensively purified and resolved from other protein kinases. In addition, the purified preparation phosphorylated a protein species, also of 68,000 apparent molecular weight, when incubated with [gamma-32P]ATP. These data are consistent with gene US3 encoding the novel protein kinase induced after infection of cells with HSV-1.
先前的研究表明,用1型单纯疱疹病毒(HSV-1)感染培养细胞后会诱导一种新型蛋白激酶产生。另外,有报道称HSV-1基因US3编码的蛋白质在氨基酸序列上与真核生物蛋白激酶家族成员相似。我们通过制备针对与US3蛋白羧基末端八个氨基酸相对应的合成寡肽的抗血清,研究了这两种观察结果是否相关。该抗血清在免疫印迹上与来自感染了HSV-1的细胞提取物中一条表观分子量为68,000的多肽发生反应。该抗血清还与一种经过大量纯化并与其他蛋白激酶分离的新型HSV-1蛋白激酶制剂中的一种分子量为68,000的蛋白强烈反应。此外,纯化制剂在与[γ-32P]ATP孵育时会使一种表观分子量也为68,000的蛋白发生磷酸化。这些数据表明基因US3编码了细胞被HSV-1感染后诱导产生的新型蛋白激酶。