Lewis R A, Watkins L, St Jeor S
Mol Cell Biochem. 1984 Nov;65(1):67-71. doi: 10.1007/BF00226020.
Studies were conducted to establish the relationship between deoxyguanosine kinase activity and human cytomegalovirus (HCMV) infection. Using both PAGE and isoelectric focusing techniques, extracts from untreated and infected cells were examined for deoxyguanosine kinase activity. The analyses resulted in identical migration rates for deoxyguanosine kinase activity in both infected and uninfected extracts. These data and kinetic studies based on apparent Km values suggest that HCMV enhanced a cellular kinase activity rather than coded for a virus specific enzyme. Furthermore, our results indicated that infected cells, like normal fibroblasts, contain two deoxyguanosine kinase activities, one of mitochondrial and another of cytosolic origin. Of particular interest was the observation that HCMV infection caused an enhancement of the mitochondrial enzymatic activity while the cytosolic activity showed no change. Deoxycytidine kinase activity which is associated with cytosolic deoxyguanosine kinase was unaffected by HCMV infection.
开展了多项研究以确定脱氧鸟苷激酶活性与人类巨细胞病毒(HCMV)感染之间的关系。使用聚丙烯酰胺凝胶电泳(PAGE)和等电聚焦技术,对未处理细胞和感染细胞的提取物进行脱氧鸟苷激酶活性检测。分析结果显示,感染细胞提取物和未感染细胞提取物中脱氧鸟苷激酶活性的迁移率相同。这些数据以及基于表观米氏常数(Km)值的动力学研究表明,HCMV增强了细胞激酶活性,而非编码一种病毒特异性酶。此外,我们的结果表明,与正常成纤维细胞一样,感染细胞含有两种脱氧鸟苷激酶活性,一种源自线粒体,另一种源自胞质溶胶。特别值得关注的是,观察发现HCMV感染导致线粒体酶活性增强,而胞质溶胶活性未发生变化。与胞质溶胶脱氧鸟苷激酶相关的脱氧胞苷激酶活性不受HCMV感染的影响。