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人巨细胞病毒DNA聚合酶与其在昆虫细胞中表达的辅助蛋白(ICP36)的物理和功能相互作用。

Physical and functional interaction of human cytomegalovirus DNA polymerase and its accessory protein (ICP36) expressed in insect cells.

作者信息

Ertl P F, Powell K L

机构信息

Department of Molecular Sciences, Wellcome Research Laboratories, Beckenham, Kent, United Kingdom.

出版信息

J Virol. 1992 Jul;66(7):4126-33. doi: 10.1128/JVI.66.7.4126-4133.1992.

Abstract

Expression of the human cytomegalovirus (HCMV) (AD169) DNA polymerase gene under the control of the polyhedrin promoter of Autographa californica nuclear polyhedrosis virus in Spodoptera frugiperda (Sf9) cells has provided a source of highly active CMV DNA polymerase. In extracts from CMV-infected cells, the CMV DNA polymerase is found strongly associated with an additional polypeptide, ICP36. This protein has been identified as the CMV homolog of the herpes simplex virus type 1 UL42 gene product and may have a similar function. We have expressed HCMV DNA polymerase and ICP36 in the same system and demonstrated that they interact to form a stable complex. Moreover, ICP36 functions to stimulate the DNA polymerase activity in a template-dependent manner. We have compared the activity of the recombinant DNA polymerase in the presence and absence of ICP36 on a number of DNA templates and measured the effect of the polymerase inhibitors phosphonoformic acid and acyclovir triphosphate.

摘要

在苜蓿银纹夜蛾核型多角体病毒多角体蛋白启动子控制下,人巨细胞病毒(HCMV)(AD169)DNA聚合酶基因在草地贪夜蛾(Sf9)细胞中的表达提供了一种高活性CMV DNA聚合酶的来源。在CMV感染细胞的提取物中,发现CMV DNA聚合酶与另一种多肽ICP36紧密相关。该蛋白已被鉴定为单纯疱疹病毒1型UL42基因产物的CMV同源物,可能具有类似功能。我们已在同一系统中表达了HCMV DNA聚合酶和ICP36,并证明它们相互作用形成稳定复合物。此外,ICP36以模板依赖的方式刺激DNA聚合酶活性。我们比较了在有和没有ICP36的情况下,重组DNA聚合酶在多种DNA模板上的活性,并测定了聚合酶抑制剂膦甲酸和阿昔洛韦三磷酸的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dec/241215/2792baaf4de2/jvirol00039-0165-a.jpg

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