Spadari S
Nucleic Acids Res. 1976 Aug;3(8):2155-67. doi: 10.1093/nar/3.8.2155.
HeLa cells contain a high M.W. form of DNA ligase which can be completely converted to a low M.W. form. Stokes radius, frictional ratio, sedimentation coefficient, molecular weight, pH dependence, and heat inactivation rate of the two forms have been studied. The major properties of the two forms of DNA ligase in HeLa cells (in particular molecular weights and pH dependence) resemble those of the "dimer" and "monomer" structures described in cultured human cells (Pedrali, G., Spadari, S., Ciarrocchi, G., Pedrini, M., Falaschi, A. (1973) Eur. J. Biochem., 39 343) . In synchronized HeLa cells, the DNA ligase shows a two fold increase during S phase and parallels the increase in the DNA synthesis rate. DNA ligase increases in parallel with viral DNA synthesis after infection of HeLa cells with vaccinia and Herpes virus but its cofactor requirements and physical properties (including the dimer leads to monomer conversion) are unchanged, suggesting that the newly formed ligase is not virus-coded.
海拉细胞含有一种高分子量形式的DNA连接酶,它可以完全转化为低分子量形式。已经研究了这两种形式的斯托克斯半径、摩擦比、沉降系数、分子量、pH依赖性和热失活率。海拉细胞中两种形式的DNA连接酶的主要特性(特别是分子量和pH依赖性)类似于培养的人类细胞中描述的“二聚体”和“单体”结构(佩德rali,G.,斯帕达里,S.,西亚罗奇,G.,佩德里尼,M.,法拉斯基,A.(1973年)欧洲生物化学杂志,39 343)。在同步化的海拉细胞中,DNA连接酶在S期增加两倍,与DNA合成速率的增加平行。在用痘苗病毒和疱疹病毒感染海拉细胞后,DNA连接酶与病毒DNA合成平行增加,但其辅因子需求和物理性质(包括二聚体向单体的转化)不变,这表明新形成的连接酶不是病毒编码的。