Paul A V, Cao X, Harris K S, Lama J, Wimmer E
Department of Molecular Genetics and Microbiology, School of Medicine, State University of New York at Stony Brook 11790-5222.
J Biol Chem. 1994 Nov 18;269(46):29173-81.
The synthesis in vitro of poly(U) on a poly(A) template with oligo(dT)15 primer by poliovirus RNA polymerase 3Dpol (280 ng/ml) is strongly stimulated (50-100 fold) by the addition of purified poliovirus polypeptide 3AB. The synthesis of product continues linearly with time for up to 90 min. The reaction with 3Dpol alone can be reactivated and similarly enhanced by the addition of 3AB at 30 min of incubation. Optimal stimulation is achieved under conditions where the concentration of 3Dpol and of template is low, when the molar ratio of 3AB to 3Dpol is about 100:1 and that of 3AB to poly(A) is about 25:1. In the presence of 3AB, the yield of product made by 3Dpol is much increased but its size is unchanged. From a number of basic proteins and peptides tested, a few were found which also exhibited limited enhancement of polymerase activity. The stimulatory effect of 3AB is probably related to its ability to bind both the template-primer, poly(A).oligo(dT)15, and 3Dpol (Molla, A., Harris, K. S., Paul, A. V., Shin, S. H., Mugavero, J., and Wimmer, E. J. (1994) J. Biol. Chem. 269, 27015-27020). RNA synthesis on purified poliovirus RNA with oligo(dT)15 primer is enhanced by 3AB about 5-10 fold, and this reaction is highly sensitive to detergent.
脊髓灰质炎病毒RNA聚合酶3Dpol(280 ng/ml)在聚(A)模板上,以寡聚(dT)15为引物体外合成聚(U)的反应,通过添加纯化的脊髓灰质炎病毒多肽3AB可得到强烈刺激(50 - 100倍)。产物的合成在长达90分钟内随时间呈线性持续。单独使用3Dpol的反应在孵育30分钟时添加3AB可被重新激活并同样得到增强。在3Dpol和模板浓度较低的条件下,当3AB与3Dpol的摩尔比约为100:1且3AB与聚(A)的摩尔比约为25:1时,可实现最佳刺激效果。在3AB存在的情况下,3Dpol产生的产物产量大幅增加但其大小不变。从测试的多种碱性蛋白质和肽中,发现有几种也表现出对聚合酶活性的有限增强作用。3AB的刺激作用可能与其结合模板引物聚(A)·寡聚(dT)15和3Dpol的能力有关(莫拉,A.,哈里斯,K. S.,保罗,A. V.,申,S. H.,穆加韦罗,J.,以及维默,E. J.(1994年)《生物化学杂志》269,27015 - 27020)。3AB可使以寡聚(dT)15为引物在纯化的脊髓灰质炎病毒RNA上进行的RNA合成增强约5 - 10倍,并且该反应对去污剂高度敏感。