首页> 外文期刊>Journal of Virology >Complex of simian virus 40 large-T antigen and host 53,000-molecular-weight protein in monkey cells.
【24h】

Complex of simian virus 40 large-T antigen and host 53,000-molecular-weight protein in monkey cells.

机译:猿猴病毒40大T抗原和寄主53,000分子量蛋白在猴细胞中的复合物。

获取原文
获取外文期刊封面目录资料

摘要

Mouse cells transformed by simian virus 40 (SV40) have been shown to contain a complex of the virus-coded large-T antigen with a host 53,000-molecular-weight (53K) protein. Initial attempts to detect a similar complex in lytically infected cells were unsuccessful, and it therefore seemed that the complex might be peculiar to transformed or abortively transformed nonpermissive cells. Immunoprecipitation of [32P]phosphate-labeled extracts of SV40-infected CV-1 African green monkey kidney cells with antibodies specific for large-T or the 53K protein revealed that the large-T-53K protein complex was formed during lytic infections. Only a minor fraction of the large-T present was associated with 53K protein, and large-T and the 53K host protein cosedimented during centrifugation through sucrose gradients. We used monospecific sera and monoclonal antibodies to study the rate of synthesis and phosphorylation of the 53K protein during lytic infections. Infection of CV-1 cells with SV40 increased the rate of synthesis of the 53K protein fivefold over that in mock-infected cells. At the same time, the rate of phosphorylation of the 53K protein increased more than 30-fold compared with control cultures. Monkey cells transformed by UV-irradiated SV40 (Gluzman et al., J. Virol. 22:256-266, 1977) also contained the large-T-53K protein complex. The formation of the complex is therefore not a peculiarity of SV40-transformed rodent cells but is a common feature of SV40 infections.
机译:已经显示由Simian病毒40(SV40)转化的小鼠细胞含有宿主53,000分子量(53K)蛋白的病毒编码的大T抗原的复合物。初步试图在裂解感染的细胞中检测类似复合物的初始尝试是不成功的,因此似乎复合物可能是转化或造成血液变化的非疾病细胞的特殊性。免疫沉淀的SV40感染的CV-1非洲绿色猴肾细胞的磷酸盐标记的提取物,具有大于T的抗体或53K蛋白质的抗体显示,在裂解感染期间形成大T-53K蛋白质复合物。只有少量的大部分大部分与53K蛋白质相关,并且通过蔗糖梯度在离心期间进行大型T和53K宿主蛋白。我们使用了单次血清和单克隆抗体来研究裂解感染期间53K蛋白的合成和磷酸化速率。具有SV40的CV-1细胞的感染增加了53K蛋白五折叠在模拟感染细胞中的合成速率。同时,与对照培养物相比,53K蛋白的磷酸化率增加了30多倍。由紫外线辐照的SV40转化的猴细胞(Gluzman等,J.Virol。22:256-266,1977)还含有大T-53K蛋白质复合物。因此,复合物的形成不是SV40转化的啮齿动物细胞的特殊性,而是SV40感染的常见特征。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号