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Proteomic profiling of lipid droplet proteins in hepatoma cell lines expressing hepatitis C virus core protein.

Proteomic profiling of lipid droplet proteins in hepatoma cell lines expressing hepatitis C virus core protein. Research Abstract Details 

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  • Proteomic profiling of lipid droplet proteins in hepatoma cell lines expressing hepatitis C virus core protein. Abstract Text:

    shigeko satoShigeko Sato,masayoshi fukasawaMasayoshi Fukasawa,yoshio yamakawaYoshio Yamakawa,tohru natsumeTohru Natsume,tetsuro suzukiTetsuro Suzuki,ikuo shojiIkuo Shoji,hideki aizakiHideki Aizaki,tatsuo miyamuraTatsuo Miyamura,masahiro nishijimaMasahiro Nishijima,

    Hepatitis C virus (HCV) core protein has been suggested to play crucial roles in the pathogeneses of liver steatosis and hepatocellular carcinomas due to HCV infection. Intracellular HCV core protein is localized mainly in lipid droplets, in which the core protein should exert its significant biological/pathological functions. In this study, we performed comparative proteomic analysis of lipid droplet proteins in core-expressing and non-expressing hepatoma cell lines. We identified 38 proteins in the lipid droplet fraction of core-expressing (Hep39) cells and 30 proteins in that of non-expressing (Hepswx) cells by 1-D-SDS-PAGE/MALDI-TOF mass spectrometry (MS) or direct nanoflow liquid chromatography-MS/MS. Interestingly, the lipid droplet fraction of Hep39 cells had an apparently lower content of adipose differentiation-related protein and a much higher content of TIP47 than that of Hepswx cells, suggesting the participation of the core protein in lipid droplet biogenesis in HCV-infected cells. Another distinct feature is that proteins involved in RNA metabolism, particularly DEAD box protein 1 and DEAD box protein 3, were detected in the lipid droplet fraction of Hep39 cells. These results suggest that lipid droplets containing HCV core protein may participate in the RNA metabolism of the host and/or HCV, affecting the pathopoiesis and/or virus replication/production in HCV-infected cells.

    Proteomic profiling of lipid droplet proteins in hepatoma cell lines expressing hepatitis C virus core protein. Publishing Authors By Initials

    s satoS Sato,m fukasawaM Fukasawa,y yamakawaY Yamakawa,t natsumeT Natsume,t suzukiT Suzuki,i shojiI Shoji,h aizakiH Aizaki,t miyamuraT Miyamura,m nishijimaM Nishijima,

    For similar biological phenomena, cell phenomena, and immunity: biological phenomena: microbiologic phenomena: viral physiology: virus replication research abstracts see: biological phenomena, cell phenomena, and immunity: biological phenomena: microbiologic phenomena: viral physiology: virus replication research

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    Proteomic profiling of lipid droplet proteins in hepatoma cell lines expressing hepatitis C virus core protein. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of biochemistry

    VOLUME: 139

    Page Numbers: 921-30

    Journal Abbreviation: J. Biochem.

    ISSN: 0021-924X

    DAY: 19

    MONTH: May

    YEAR: 2006

    Proteomic profiling of lipid droplet proteins in hepatoma cell lines expressing hepatitis C virus core protein. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 376600

    Proteomic profiling of lipid droplet proteins in hepatoma cell lines expressing hepatitis C virus core protein. Keywords Mesh Terms:

    KEYWORDS: Virus Replication

    MESH TERMS: isolation & purification

    Chemical & Substance for Abstract: Proteomic profiling of lipid droplet proteins in hepatoma cell lines expressing hepatitis C virus core protein. Information

    Substance Name: DDX3X protein, human

    Registry Number: EC 3.6.1.-

    Grant and Affiliation Information for Proteomic profiling of lipid droplet proteins in hepatoma cell lines expressing hepatitis C virus core protein.

    AFFILIATION: Department of Biochemistry and Cell Biology and Department of Virology II, National Institute of Infectious Diseases, Tokyo 162-8640.

    Country: Japan

    Japan Research PublicationJapan Research Publication

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    MEDLINETA: J Biochem

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