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烟草脉斑驳病毒小核内含蛋白中的一个酪氨酸残基将病毒基因组连接蛋白(VPg)与病毒RNA相连。

A tyrosine residue in the small nuclear inclusion protein of tobacco vein mottling virus links the VPg to the viral RNA.

作者信息

Murphy J F, Rychlik W, Rhoads R E, Hunt A G, Shaw J G

机构信息

Department of Plant Pathology, University of Kentucky, Lexington 40546-0091.

出版信息

J Virol. 1991 Jan;65(1):511-3. doi: 10.1128/JVI.65.1.511-513.1991.

Abstract

The identity of the amino acid residue that links the VPg of the potyvirus tobacco vein mottling virus (TVMV) to the viral RNA was determined. 32P-labeled TVMV RNA was digested with RNase A and micrococcal nuclease. The resulting 32P-labeled VPg was isolated and partially hydrolyzed with 6 N HCl at 110 degrees C for 2 h. Analysis by thin-layer electrophoresis revealed the presence of [32P]phosphotyrosine but not [32P]phosphoserine or [32P]phosphothreonine. Another preparation of TVMV RNA was treated with endoproteinase Lys-C, and the resulting peptide-RNA was purified by sodium dodecyl sulfate-sucrose gradient centrifugation. The sequence of the N-terminal 15 amino acid residues of the peptide, when compared with the RNA-derived amino acid sequence of the TVMV polyprotein, demonstrated that the peptide occurs in the small nuclear inclusion protein. These data suggest that Tyr-1860 of the polyprotein is the amino acid residue that links the TVMV VPg to the viral RNA.

摘要

确定了将马铃薯Y病毒属烟草脉斑驳病毒(TVMV)的VPg与病毒RNA连接起来的氨基酸残基的身份。用核糖核酸酶A和微球菌核酸酶消化32P标记的TVMV RNA。分离得到的32P标记的VPg,并在110℃下用6N盐酸部分水解2小时。薄层电泳分析显示存在[32P]磷酸酪氨酸,但不存在[32P]磷酸丝氨酸或[32P]磷酸苏氨酸。用内肽酶Lys-C处理另一批TVMV RNA制剂,所得肽-RNA通过十二烷基硫酸钠-蔗糖梯度离心纯化。将该肽N端15个氨基酸残基的序列与TVMV多聚蛋白的RNA衍生氨基酸序列进行比较,结果表明该肽存在于小核内含蛋白中。这些数据表明,多聚蛋白的Tyr-1860是将TVMV VPg与病毒RNA连接起来的氨基酸残基。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6085/240548/ff25778d45e4/jvirol00044-0534-a.jpg

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