Sarkar S N, Sen G C
Department of Molecular Biology, The Lerner Research Institute, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, Ohio, 44195, USA.
Methods. 1998 Jul;15(3):233-42. doi: 10.1006/meth.1998.0627.
2',5'-Oligoadenylate [2-5(A)] synthetases are a family of interferon-induced enzymes that polymerize ATP into 2'-5'-linked oligoadenylates in the presence of double-stranded RNA (dsRNA), their cofactor. The 2-5(A) molecules, in turn, activate the latent ribonuclease RNase L by promoting its dimerization. The 2-5(A) synthetase pathway has been implicated in interferon's antiviral and anticellular activities. In addition to their interesting cellular properties, these enzymes are also enzymologically interesting because they are the only known template and primer independent nucleotide (DNA or RNA)polymerases that synthesize 2'-5'-linked oligonucleotides. Moreover, their mode of activation by dsRNA remains unknown. In the past, biochemical and structure-function studies have been hampered by the lack of a convenient system for expressing recombinant 2-5(A) synthetases. These proteins are toxic to mammalian cells, probably because of RNase L activation, and proteins produced in bacteria do not have full enzymatic activity. To circumvent these problems, we have developed a baculovirus-insect cell system for high-yield expression of the small and medium isozymes. Here, methods are described for the production, purification, and characterization of the mouse small (9-2) (S. K. Ghosh, J. Kusari, S. K. Bandyopadhyay, H. Samanta, R. Kumar, and G. C. Sen, 1991, J. Biol. Chem. 266, 15293-15299) and human medium (P69) (I. Marie and A. G. Hovanessian, 1992, J. Biol. Chem. 267, 9933-9939) 2-5(A) synthetase isozymes and their mutants using the insect cell system. We also report methods for studying 2-5(A) synthetase-dsRNA interactions and protein-protein interactions among the subunits of the two isozymes.
2',5'-寡腺苷酸[2-5(A)]合成酶是一类由干扰素诱导产生的酶,在其辅因子双链RNA(dsRNA)存在的情况下,可将ATP聚合成2'-5'-连接的寡腺苷酸。反过来,2-5(A)分子通过促进潜伏的核糖核酸酶RNase L二聚化来激活它。2-5(A)合成酶途径与干扰素的抗病毒和抗细胞活性有关。除了其有趣的细胞特性外,这些酶在酶学上也很有趣,因为它们是唯一已知的不依赖模板和引物的核苷酸(DNA或RNA)聚合酶,可合成2'-5'-连接的寡核苷酸。此外,它们被dsRNA激活的模式仍然未知。过去,生化和结构功能研究因缺乏表达重组2-5(A)合成酶的便捷系统而受到阻碍。这些蛋白质对哺乳动物细胞有毒性,可能是由于RNase L的激活,而在细菌中产生的蛋白质没有完全的酶活性。为了规避这些问题,我们开发了一种杆状病毒-昆虫细胞系统,用于高产表达中小同工酶。本文描述了使用昆虫细胞系统生产、纯化和鉴定小鼠小(9-2)(S.K.戈什、J.库萨里、S.K.班迪奥帕德希亚、H.萨曼塔、R.库马尔和G.C.森,1991年,《生物化学杂志》266卷,第15293 - 15299页)和人中等(P69)(I.玛丽和A.G.霍瓦内西安,1992年,《生物化学杂志》267卷,第9933 - 9939页)2-5(A)合成酶同工酶及其突变体的方法。我们还报告了研究2-5(A)合成酶-dsRNA相互作用以及两种同工酶亚基之间蛋白质-蛋白质相互作用的方法。