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在被猿猴病毒40有效感染的细胞中鉴定病毒诱导蛋白。

Identification of virus-induced proteins in cells productively infected with simian virus 40.

作者信息

Fischer H, Sauer G

出版信息

J Virol. 1972 Jan;9(1):1-9. doi: 10.1128/JVI.9.1.1-9.1972.

Abstract

The number and molecular weight of the structural polypeptides of highly purified simian virus 40 (SV40) were determined by polyacrylamide gel electrophoresis. Six different polypeptides were found, two of which (VP1 and VP2) comprise the bulk of the viral capsid proteins. The pattern of protein synthesis in productively infected CV-1 cells was studied by sodium dodecyl sulfate polyacrylamide gel electrophoresis. Identification of virus-induced proteins in the infected CV-1 cells was achieved in double-labeling experiments by electrophoresis with purified labeled SV40 capsid proteins. Four of these proteins (VP1 and VP4) could be classified as components of the virion because their synthesis occurred after the onset of viral deoxyribonucleic acid (DNA) replication and because they were inhibited by arabinofuranosylcytosine (ara-C). Appearance of two other virus-induced proteins was not prevented by ara-C; one of them did not comigrate in the electrophoresis with purified virion polypeptides, and both could be detected before the onset of viral DNA synthesis. These latter two proteins were classified on the basis of these criteria as nonvirion capsid proteins (NCVP1 and NCVP2).

摘要

通过聚丙烯酰胺凝胶电泳测定了高度纯化的猴病毒40(SV40)结构多肽的数量和分子量。发现了六种不同的多肽,其中两种(VP1和VP2)构成了病毒衣壳蛋白的主要部分。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳研究了有效感染的CV-1细胞中的蛋白质合成模式。在双标记实验中,通过与纯化的标记SV40衣壳蛋白一起电泳,确定了感染的CV-1细胞中病毒诱导的蛋白质。其中四种蛋白质(VP1和VP4)可归类为病毒粒子的成分,因为它们的合成发生在病毒脱氧核糖核酸(DNA)复制开始之后,并且因为它们被阿拉伯糖胞苷(ara-C)抑制。ara-C并不能阻止另外两种病毒诱导蛋白的出现;其中一种在电泳中与纯化的病毒粒子多肽不共迁移,并且在病毒DNA合成开始之前都能被检测到。根据这些标准,后两种蛋白质被归类为非病毒粒子衣壳蛋白(NCVP1和NCVP2)。

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Proc Natl Acad Sci U S A. 1968 Aug;60(4):1239-46. doi: 10.1073/pnas.60.4.1239.
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