首页> 美国卫生研究院文献>Viruses >Cloning and Characterization of Sf9 Cell Lamin and the Lamin Conformational Changes during Autographa californica multiple nucleopolyhedrovirus Infection
【2h】

Cloning and Characterization of Sf9 Cell Lamin and the Lamin Conformational Changes during Autographa californica multiple nucleopolyhedrovirus Infection

机译:Sf9细胞层粘连蛋白的克隆鉴定及其在加利福尼亚州自传体多核多角体病毒感染期间的层粘连蛋白构象变化

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

At present, the details of lamina alterations after baculovirus infection remain elusive. In this study, a lamin gene in the Sf9 cell line of Spodoptera frugiperda was cloned. The open reading frame (orf) of the Sf9 lamin was 1860 bp and encoded a protein with a molecular weight of 70 kDa. A transfection assay with a red fluorescence protein (rfp)-lamin fusion protein indicated that Sf9 lamin was localized in the nuclear rim. Transmission electron microscopy observations indicated that Autographa californica multiple nucleopolyhedrovirus (AcMNPV) nucleocapsids may pass through the nuclear envelope. Immunofluorescence assay indicated that the lamina showed a ruffled staining pattern with the formation of invaginations in the Sf9 cells infected with AcMNPV, while it was evenly distributed at the nuclear periphery of mock-infected cells. Western blotting results indicated that the total amount of lamin in the baculovirus-infected Sf9 cells was significantly decreased compared with the mock-infected cells. These results imply that AcMNPV infection induces structural and biochemical rearrangements of lamina of Sf9 cells.
机译:目前,杆状病毒感染后椎板改变的细节仍然难以捉摸。在这项研究中,在草地贪夜蛾的Sf9细胞系中克隆了一种lamin基因。 Sf9层蛋白的开放阅读框(orf)为1860 bp,编码分子量为70 kDa的蛋白质。用红色荧光蛋白(rfp)-lamin融合蛋白进行的转染分析表明,Sf9核纤层蛋白位于核环中。透射电子显微镜的观察结果表明,加州致癌的Autographa californica多核多角体病毒(AcMNPV)核衣壳可能会穿过核膜。免疫荧光分析表明,在被AcMNPV感染的Sf9细胞中,薄层显示出皱纹的染色模式,并形成内陷,而在模拟感染细胞的核周边均匀分布。 Western印迹结果表明,与模拟感染的细胞相比,杆状病毒感染的Sf9细胞中层粘连蛋白的总量明显减少。这些结果暗示AcMNPV感染诱导Sf9细胞的层板的结构和生化重排。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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