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马尾松毛虫四病毒RNA依赖的RNA聚合酶的表达与鉴定

Expression and characterization of RNA-dependent RNA polymerase of Dendrolimus punctatus tetravirus.

作者信息

Zhou Liang, Zhang Jiamin, Wang Xiaochun, Jiang Hong, Yi Fuming, Hu Yuanyang

机构信息

State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, Hubei 430072, P R China.

出版信息

J Biochem Mol Biol. 2006 Sep 30;39(5):571-7. doi: 10.5483/bmbrep.2006.39.5.571.

Abstract

Dendrolimus punctatus tetravirus (DpTV) has been identified as a new member of the genus Omegatetravirus of the family Tetraviridae that may be related serologically to Nudaurelia capensis virus (NomegaV). To establish the function of DpTV RNA genome and to better understand the mechanism of viral replication, the putative RNA-dependent RNA polymerase (RdRp) domain has been cloned and expressed in Escherichia coli. The recombinant protein was purified on a Ni-chelating HisTrap affinity column and demonstrated to initiate viral RNA synthesis in a primer-independent manner but not by terminal nucleotidyle transferase activity in the presence of Mg2+ and RNA template. Mutation of the GDD to GAA interferes with the residues at the polymerase active site and metal ions, and thus renders the polymerase inactive.

摘要

马尾松毛虫四病毒(DpTV)已被鉴定为四病毒科ω四病毒属的一个新成员,在血清学上可能与非洲野蚕核型多角体病毒(NomegaV)相关。为了确定DpTV RNA基因组的功能并更好地理解病毒复制机制,已在大肠杆菌中克隆并表达了假定的RNA依赖性RNA聚合酶(RdRp)结构域。重组蛋白在镍螯合HisTrap亲和柱上纯化,并证明其能以不依赖引物的方式起始病毒RNA合成,但在Mg2+和RNA模板存在的情况下不能通过末端核苷酸转移酶活性起始合成。将GDD突变为GAA会干扰聚合酶活性位点和金属离子处的残基,从而使聚合酶失活。

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