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感染亚洲1型口蹄疫病毒的BHK - 21细胞的定量蛋白质组学分析

Quantitative Proteomic Analysis of BHK-21 Cells Infected with Foot-and-Mouth Disease Virus Serotype Asia 1.

作者信息

Guo Hui-Chen, Jin Ye, Han Shi-Chong, Sun Shi-Qi, Wei Yan-Quan, Liu Xian-Ji, Feng Xia, Liu Ding Xiang, Liu Xiang-Tao

机构信息

State Key Laboratory of Veterinary Etiological Biology and OIE/National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu, China.

Guangzhou Fitgene Biotechnology Co. Ltd. Guangzhou International Business Incubator A110, Guangzhou, Guangdong, China.

出版信息

PLoS One. 2015 Jul 10;10(7):e0132384. doi: 10.1371/journal.pone.0132384. eCollection 2015.

Abstract

Stable isotope labeling with amino acids in cell culture (SILAC) was used to quantitatively study the host cell gene expression profile, in order to achieve an unbiased overview of the protein expression changes in BHK-21 cells infected with FMDV serotype Asia 1. The SILAC-based approach identified overall 2,141 proteins, 153 of which showed significant alteration in the expression level 6 h post FMDV infection (57 up-regulated and 96 down-regulated). Among these proteins, six cellular proteins, including three down-regulated (VPS28, PKR, EVI5) and three up-regulated (LYPLA1, SEC62 and DARs), were selected according to the significance of the changes and/or the relationship with PKR. The expression level and pattern of the selected proteins were validated by immunoblotting and confocal microscopy. Furthermore, the functions of these cellular proteins were assessed by small interfering RNA-mediated depletion, and their functional importance in the replication of FMDV was demonstrated by western blot, reverse transcript PCR (RT-PCR) and 50% Tissue Culture Infective Dose (TCID50). The results suggest that FMDV infection may have effects on the expression of specific cellular proteins to create more favorable conditions for FMDV infection. This study provides novel data that can be utilized to understand the interactions between FMDV and the host cell.

摘要

采用细胞培养中氨基酸的稳定同位素标记法(SILAC)定量研究宿主细胞基因表达谱,以全面了解感染亚洲1型口蹄疫病毒(FMDV)的BHK-21细胞中蛋白质表达的变化。基于SILAC的方法共鉴定出2141种蛋白质,其中153种在FMDV感染后6小时表达水平出现显著变化(57种上调,96种下调)。在这些蛋白质中,根据变化的显著性和/或与PKR的关系,选择了6种细胞蛋白,包括3种下调蛋白(VPS28、PKR、EVI5)和3种上调蛋白(LYPLA1、SEC62和DARs)。通过免疫印迹和共聚焦显微镜对所选蛋白质的表达水平和模式进行了验证。此外,通过小干扰RNA介导的敲低评估了这些细胞蛋白的功能,并通过蛋白质印迹、逆转录PCR(RT-PCR)和50%组织培养感染剂量(TCID50)证明了它们在FMDV复制中的功能重要性。结果表明,FMDV感染可能会影响特定细胞蛋白的表达,为FMDV感染创造更有利的条件。本研究提供了新的数据,可用于了解FMDV与宿主细胞之间的相互作用。

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