Marton A, Jean D, Delbecchi L, Simmons D T, Bourgaux P
Département de Microbiologie, Faculté de Médicine, Université de Sherbrooke, Québec, Canada.
Nucleic Acids Res. 1993 Apr 25;21(8):1689-95. doi: 10.1093/nar/21.8.1689.
Purified preparations of simian virus 40 (SV40) large tumor antigen (LT) from three different sources, including LT expressed from a recombinant baculovirus, were found to relax negatively supercoiled cyclic DNA molecules, whether or not they contained SV40 sequences. Relaxation was stimulated by MgCl2 but not by ATP, and inhibited by camptothecin, suggesting the involvement of an enzymatic activity similar to that of topoisomerase I (topo I). However, the pH requirements for relaxation by respectively LT and topo I are different. Also, antibodies reacting with LT inhibited relaxation by preparations of LT but not topo I, whereas antibodies inhibiting relaxation by topo I had no effect on relaxation by LT. Reconstruction experiments suggested that both procedures used to purify LT, immunoaffinity chromatography and DEAE-Sepharose chromatography, separate topo I from LT. Finally, relaxing activity was found in over 40 preparations of LT, and in the few instances where activity could not be found, it probably had been lost during storage, rather than absent from the start. Whereas these results seem to exclude that the activity being detected is that of a contaminant of LT, they would be consistent with this activity being that of a stable topo-LT complex, or else intrinsic to LT itself.
从三种不同来源纯化得到的猿猴病毒40(SV40)大T抗原(LT)制剂,包括从重组杆状病毒表达的LT,无论是否含有SV40序列,都能使负超螺旋环状DNA分子松弛。MgCl2能刺激松弛反应,但ATP不能,喜树碱可抑制松弛反应,这表明存在一种类似于拓扑异构酶I(topo I)的酶活性。然而,LT和topo I引起松弛反应的pH要求不同。此外,与LT反应的抗体可抑制LT制剂引起的松弛反应,但不能抑制topo I引起的松弛反应,而抑制topo I引起松弛反应的抗体对LT引起的松弛反应没有影响。重建实验表明,用于纯化LT的免疫亲和层析和DEAE-琼脂糖层析这两种方法都能将topo I与LT分离。最后,在40多种LT制剂中都发现了松弛活性,在少数未发现活性的情况下,活性可能是在储存过程中丧失的,而不是一开始就不存在。虽然这些结果似乎排除了所检测到的活性是LT污染物的活性,但它们与这种活性是稳定的topo-LT复合物的活性或LT本身固有的活性是一致的。