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棉尾兔疱疹病毒CTHV诱导的DNA结合蛋白

DNA-binding proteins induced by the cottontail rabbit herpesvirus CTHV.

作者信息

Cajean-Feroldi C, Laithier M, Foulon T, Sheldrick P

机构信息

Institut de Recherches Scientifiques sur le Cancer, Villejuif, France.

出版信息

J Gen Virol. 1988 Sep;69 ( Pt 9):2277-89. doi: 10.1099/0022-1317-69-9-2277.

Abstract

Several new polypeptides were detected in cells infected with CTHV, a cottontail rabbit herpesvirus. All of them (Mr 150K, 110K, 93K, 83K, 75K and 35K) accumulated in the nucleus during the infectious cycle, and all except the 150K species bound to DNA-cellulose affinity columns in low-salt buffers. Polyclonal antisera prepared against the 35K DNA-binding protein also recognized the 75K species. Although the 75K protein could be detected earlier in infection than the 35K protein, late in the infectious cycle the latter increased to an abundance approaching that of cellular histones. Treatment of partially purified virions with a non-ionic detergent indicated that the 35K protein, but not the 75K protein, is a component of capsid/tegument structures. The anti-35K/75K serum did not cross-react with herpesvirus sylvilagus virion proteins, which, in an electrophoretic comparison, exhibited both similarities to and differences from the virion proteins of CTHV. Labelling of CTHV-infected cells with [32P]orthophosphate revealed the presence of phosphoproteins electrophoretically comigrating with the 93K, 83K, 75K and 35K proteins.

摘要

在感染棉尾兔疱疹病毒(CTHV)的细胞中检测到了几种新的多肽。所有这些多肽(分子量分别为150K、110K、93K、83K、75K和35K)在感染周期中都在细胞核中积累,除了150K的多肽外,其他多肽在低盐缓冲液中都能与DNA纤维素亲和柱结合。针对35K DNA结合蛋白制备的多克隆抗血清也能识别75K的多肽。虽然在感染过程中75K蛋白比35K蛋白更早被检测到,但在感染周期后期,35K蛋白的丰度增加,接近细胞组蛋白的丰度。用非离子去污剂处理部分纯化的病毒粒子表明,35K蛋白是衣壳/被膜结构的一个组成部分,而75K蛋白不是。抗35K/75K血清与森林兔疱疹病毒的病毒粒子蛋白不发生交叉反应,在电泳比较中,森林兔疱疹病毒的病毒粒子蛋白与CTHV的病毒粒子蛋白既有相似之处,也有不同之处。用[32P]正磷酸盐标记CTHV感染的细胞,发现存在与93K、83K、75K和35K蛋白电泳迁移率相同的磷蛋白。

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