Karlström A R, Neumüller M, Gronowitz J S, Källander C F
Department of Medical Virology, Uppsala University, Sweden.
Mol Cell Biochem. 1990 Jan 18;92(1):23-35. doi: 10.1007/BF00220716.
Both thymidine kinase (TK) and DNA polymerase (DNAp) are present in measurable amounts in human serum. Even though the use of TK as a clinical marker is rapidly increasing there has been no attempt to characterize the serum TK in a wider extent, i.e.; with respect to Mw or other biochemical parameters. Therefore sera with high TK or DNAp activities derived from patients with cytomegalovirus (CMV) infection, B12-deficiency and leukaemia were fractionated by gel exclusion chromatography. The TK activity eluted as two peaks, one major TK activity with an apparent molecular weight (Mw) or 730 kD and one minor TK activity corresponding to a Mw of 58 kD. The amount of TK activity at 58 kD varied between 7 and 23% of total activity, depending on the serum fractionated. The DNAp activity in sera from patients with malignant disease and B12 deficiency eluted as a single peak corresponding to a Mw of 240 kD. A DNAp with a different Mw (greater than 1000 kD) was recovered from 1 of 3 investigated immunosuppressed patients with CMV infection. A similar pattern of enzyme forms was observed when sera were separated by glycerol gradient centrifugation. The effect of high salt and various reaction solution components on the enzymes were studied. The only condition found that affected the molecular forms of TK was the state of reduction. Incubation of sera with high concentrations of dithioerythritol (DTE) (400 mM) prior to separation transferred all serum TK to the 58 kD form, it also converted most of the serum DNAp from the 240 kD form to a smaller form (56 kD) without affecting the total recovery of enzymatic activity. The reaction product from both TK forms was exclusively monophosphate and none of the TK forms could efficiently utilize cytidine triphosphate as phosphate donor. The substrate kinetics of the small serum TK fraction was identical with those of an enzyme with similar size purified from proliferating HeLa cells, indicating that both serum TK activities are forms of TK 1, the proliferation associated cellular isozyme.
胸苷激酶(TK)和DNA聚合酶(DNAp)在人血清中均有可测量的含量。尽管将TK用作临床标志物的应用正在迅速增加,但尚未有人尝试在更广泛的范围内对血清TK进行表征,即:关于分子量(Mw)或其他生化参数。因此,对来自巨细胞病毒(CMV)感染、维生素B12缺乏和白血病患者的具有高TK或DNAp活性的血清进行凝胶排阻色谱分离。TK活性以两个峰洗脱,一个主要的TK活性,表观分子量(Mw)为730 kD,一个次要的TK活性,对应Mw为58 kD。58 kD处的TK活性量占总活性的7%至23%,具体取决于所分离的血清。恶性疾病和维生素B12缺乏患者血清中的DNAp活性以对应Mw为240 kD的单峰洗脱。从3例接受调查的CMV感染免疫抑制患者中的1例中回收了一种不同Mw(大于1000 kD)的DNAp。当通过甘油梯度离心分离血清时,观察到了类似模式的酶形式。研究了高盐和各种反应溶液成分对这些酶的影响。发现唯一影响TK分子形式的条件是还原状态。在分离前用高浓度的二硫苏糖醇(DTE)(400 mM)孵育血清,可将所有血清TK转化为58 kD形式,它还将大多数血清DNAp从240 kD形式转化为较小的形式(56 kD),而不影响酶活性的总回收率。两种TK形式的反应产物均仅为单磷酸,且没有一种TK形式能够有效地利用三磷酸胞苷作为磷酸供体。小血清TK组分的底物动力学与从增殖的HeLa细胞中纯化的大小相似的酶相同,表明两种血清TK活性均为TK 1的形式,即与增殖相关的细胞同工酶。