Deiman B A, Séron K, Jaspars E M, Pleij C W
Leiden Institute of Chemistry, Leiden University, The Netherlands.
J Virol Methods. 1997 Mar;64(2):181-95. doi: 10.1016/s0166-0934(96)02166-0.
The RNA-dependent RNA polymerase (RdRp) of turnip yellow mosaic virus (TYMV) was isolated by a simple, new method. An active, template-dependent and specific enzyme was obtained. Although the genomic RNA of TYMV could not be transcribed completely during an in vitro RdRp assay, a complete double-stranded product was obtained when a 3' terminal RNA fragment of 83 nucleotides was used as a template. The reaction product was identified as being of negative polarity by complete digestion with ribonuclease T1. Antibodies directed to part of the N-terminal (Ab140) or C-terminal (Ab66) in vitro autocleavage products of the large non-structural polyprotein of TYMV, could both partially inhibit RdRp activity. Further purification of the RdRp preparation by ion-exchange chromatography resulted in two activity peaks with different protein compositions. Both peak fractions retained high specificity for transcription of TYMV RNA. A protein of approximately 115 kDa was detected by both Ab140 and Ab66.
采用一种简单的新方法分离了芜菁黄花叶病毒(TYMV)的RNA依赖性RNA聚合酶(RdRp)。获得了一种具有活性、依赖模板且具有特异性的酶。尽管在体外RdRp检测过程中TYMV的基因组RNA无法完全转录,但当使用一个83个核苷酸的3'末端RNA片段作为模板时,获得了完整的双链产物。通过用核糖核酸酶T1完全消化,反应产物被鉴定为负极性。针对TYMV大的非结构多蛋白体外自切割产物的N端部分(Ab140)或C端部分(Ab66)的抗体,均可部分抑制RdRp活性。通过离子交换色谱进一步纯化RdRp制剂,得到了两个具有不同蛋白质组成的活性峰。两个峰级分对TYMV RNA转录均保持高特异性。Ab140和Ab66均检测到一种约115 kDa的蛋白质。