An interactome map of the nucleocapsid protein from a highly pathogenic North American porcine reproductive and respiratory syndrome virus strain generated using SILAC-based quantitative proteomics

被引:44
作者
Jourdan, Stefanie S. [1 ,2 ]
Osorio, Fernando [3 ]
Hiscox, Julian A. [1 ,2 ]
机构
[1] Univ Leeds, Inst Mol & Cellular Biol, Fac Biol Sci, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Leeds, Astbury Ctr Struct Mol Biol, Leeds LS2 9JT, W Yorkshire, England
[3] Univ Nebraska, Sch Vet & Biomed Sci, Lincoln, NE USA
关键词
Bioinformatics; MASCOT; Microbiology; Multiprotein complex; Stable isotope labelling; NUCLEAR RIBONUCLEOPROTEIN A1; MOUSE HEPATITIS-VIRUS; INFECTIOUS-BRONCHITIS VIRUS; LOCALIZATION SIGNAL; CELLULAR-PROTEINS; RNA; CORONAVIRUS; NUCLEOLUS; TRANSCRIPTION; CELLS;
D O I
10.1002/pmic.201100469
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Positive strand RNA viruses replicate in the cytoplasm of an infected cell and encode nucleocapsid proteins. These proteins function to promote encapsidation of the RNA genome and virus particle assembly as well as playing potential roles in viral RNA synthesis. Nucleocapsid proteins can also associate with cellular proteins and signaling cascades. The arterivirus nucleocapsid (N) protein is no exception and localizes to both the cytoplasm and the nucleolus in virus-infected cells. This study generated an interactome map of the N protein from a highly virulent North American strain of porcine reproductive and respiratory syndrome virus (PRRSV). This is a major pathogen of swine resulting in significant morbidity and mortality. Crucial to the study was the use of SILAC coupled to affinity purification using GFP-traps and LC-MS/MS. This approach has not been applied before to the investigation of host/viral protein interactomes and this study revealed that the PRRSV N protein interacts with the host cell protein synthesis machinery especially at the level of translation initiation as well as with the RNA post-transcriptional modification machinery. Applications of the dataset can include studies of virus/host interactions and the design of live attenuated recombinant vaccines.
引用
收藏
页码:1015 / 1023
页数:9
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