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嘧啶衍生物对感染脑心肌炎病毒的福格和伦德(FL)细胞的RNA依赖性RNA聚合酶的影响。

Effects of pyrimidine derivatives on RNA-dependent RNA polymerase of mengovirus-infected Fogh and Lund (FL) cells.

作者信息

Tonew E, Fahlabusch B

出版信息

J Gen Virol. 1977 Jan;34(1):37-45. doi: 10.1099/0022-1317-34-1-37.

Abstract

Two newly synthesized pyrimidine derivatives were found to possess antiviral activity against Mengovirus in Fogh and Lund (FL) cells and in a cell-free system. The inhibitory effect on RNA-dependent RNA polymerase of Mengovirus-infected FL cells was assayed using 14C-UTP as precursor. Addition of 50 or 100 muM of the inhibitors in a cell-free system of crude enzyme and nucleoside triphosphate medium for 60 min incubation at 37 degrees C resulted in about 40 to 60% lower counting rates for drug-treated reaction mixtures. The analysis of the polymerase synthesis product (virus RNA extracted from the cell-free reaction mixture and deproteinized by the phenol-SDS method) was carried out by means of agarose-acrylamide gel electrophoresis. The main finding was a reduction of single-stranded Mengovirus RNA (RNase-sensitive and LiCl-precipitable). The rates of synthesis of the replicative intermediate (LiCl-precipitable) and the replicative form of RNA (LiCl-soluble) were not significantly influenced.

摘要

发现两种新合成的嘧啶衍生物在福格和伦德(FL)细胞以及无细胞系统中对门戈病毒具有抗病毒活性。以14C-UTP作为前体,测定了其对感染门戈病毒的FL细胞中依赖RNA的RNA聚合酶的抑制作用。在含有粗酶和核苷三磷酸培养基的无细胞系统中加入50或100μM抑制剂,于37℃孵育60分钟,结果药物处理的反应混合物的计数率降低了约40%至60%。通过琼脂糖-丙烯酰胺凝胶电泳对聚合酶合成产物(从无细胞反应混合物中提取并用酚-SDS法脱蛋白的病毒RNA)进行分析。主要发现是单链门戈病毒RNA(对RNase敏感且可被LiCl沉淀)减少。复制中间体(可被LiCl沉淀)和RNA复制形式(可被LiCl溶解)的合成速率未受到显著影响。

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