中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Global quantitative proteomic analysis profiles host protein expression in response to sendai virus infection

文献类型:期刊论文

作者Zhu, Sheng-Lin1; Chen, Xi2,3; Wang, Liang-Jie4; Wan, Wei-Wei1; Xin, Qi-Lin1; Wang, Wei1; Xiao, Gengfu1; Zhang, Lei-Ke1
刊名Proteomics
出版日期2017-03-01
卷号17期号:5页码:13
ISSN号1615-9853
关键词Innate immune response Quantitative proteomics Sendai virus Virus-host interaction
DOI10.1002/pmic.201600239
通讯作者Zhang, lei-ke(zhangleike@wh.iov.cn)
英文摘要Sendai virus (sev) is an enveloped nonsegmented negative-strand rna virus that belongs to the genus respirovirus of the paramyxoviridae family. as a model pathogen, sev has been extensively studied to define the basic biochemical and molecular biologic properties of the paramyxoviruses. in addition, sev-infected host cells were widely employed to uncover the mechanism of innate immune response. to identify proteins involved in the sev infection process or the sev-induced innate immune response process, system-wide evaluations of sev-host interactions have been performed. cdna microarray, sirna screening and phosphoproteomic analysis suggested that multiple signaling pathways are involved in sev infection process. here, to study sev-host interaction, a global quantitative proteomic analysis was performed on sev-infected hek 293t cells. a total of 4699 host proteins were quantified, with 742 proteins being differentially regulated. bioinformatics analysis indicated that regulated proteins were mainly involved in "interferon type i (ifn-i) signaling pathway" and "defense response to virus," suggesting that these processes play roles in sev infection. further rnai-based functional studies indicated that the regulated proteins, tripartite motif (trim24) and trim27, affect sev-induced ifn-i production. our data provided a comprehensive view of host cell response to sev and identified host proteins involved in the sev infection process or the sev-induced innate immune response process.
WOS关键词NF-KAPPA-B ; TRANSCRIPTION FACTOR ACTIVATION ; CELLULAR ANTIVIRAL RESPONSE ; NEWCASTLE-DISEASE VIRUS ; I INTERFERON INDUCTION ; EPITHELIAL-CELLS ; K63-LINKED UBIQUITINATION ; GENE-EXPRESSION ; DENDRITIC CELLS ; RIG-I
WOS研究方向Biochemistry & Molecular Biology
WOS类目Biochemical Research Methods ; Biochemistry & Molecular Biology
语种英语
出版者WILEY
WOS记录号WOS:000397390800004
URI标识http://www.irgrid.ac.cn/handle/1471x/2373455
专题武汉病毒研究所
通讯作者Zhang, Lei-Ke
作者单位1.Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Hubei, Peoples R China
2.Wuhan Inst Biotechnol, Lab Biol Mass Spectromet, Wuhan, Peoples R China
3.Wuhan Univ, Med Res Inst, Wuhan, Peoples R China
4.Hubei Univ Educ, Sch Chem & Life Sci, Wuhan, Peoples R China
推荐引用方式
GB/T 7714
Zhu, Sheng-Lin,Chen, Xi,Wang, Liang-Jie,et al. Global quantitative proteomic analysis profiles host protein expression in response to sendai virus infection[J]. Proteomics,2017,17(5):13.
APA Zhu, Sheng-Lin.,Chen, Xi.,Wang, Liang-Jie.,Wan, Wei-Wei.,Xin, Qi-Lin.,...&Zhang, Lei-Ke.(2017).Global quantitative proteomic analysis profiles host protein expression in response to sendai virus infection.Proteomics,17(5),13.
MLA Zhu, Sheng-Lin,et al."Global quantitative proteomic analysis profiles host protein expression in response to sendai virus infection".Proteomics 17.5(2017):13.

入库方式: iSwitch采集

来源:武汉病毒研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。