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在肝外来源的细胞系中检测乙肝病毒前S表面蛋白的细胞特异性受体。

Detection of cellular receptors specific for the hepatitis B virus preS surface protein on cell lines of extrahepatic origin.

作者信息

Park J H, Choi E A, Cho E W, Lee Y J, Park J M, Na S Y, Kim K L

机构信息

Protein Engineering Laboratory, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Yusong, Taejon, 305-600, South Korea.

出版信息

Biochem Biophys Res Commun. 2000 Oct 14;277(1):246-54. doi: 10.1006/bbrc.2000.3661.

Abstract

Hepatitis B virus infection is primarily mediated by the interaction of the preS region of the viral envelope protein with its still unknown cellular receptor. Using recombinantly expressed preS proteins, the distribution of preS-binding receptors on cell lines from extrahepatic origins was determined by immunofluorescence and flow cytometry. In contrast to human liver cell lines, most cell lines from extrahepatic origins did not bind preS proteins. Nevertheless, exceptions were found in the bone marrow-derived cell line, KG-1, and the osteogenic sarcoma cell line SaOS-2, as well as in the previously reported EBV-transformed B-cell line, Wa. To determine the biochemical nature of these receptors, Wa-cells were cell surface biotinylated and the preS-binding receptors were isolated by immunoprecipitation. A specific band with a molecular weight of approximately 30 kDa was identified in a SDS-polyacrylamide gel, which further characterization is expected to provide clues regarding the infection mechanism of HBV in hepatic- and extra-hepatic cells.

摘要

乙型肝炎病毒感染主要由病毒包膜蛋白的前S区域与其仍未知的细胞受体相互作用介导。利用重组表达的前S蛋白,通过免疫荧光和流式细胞术确定了肝外来源细胞系上前S结合受体的分布。与人类肝细胞系不同,大多数肝外来源的细胞系不结合前S蛋白。然而,在骨髓来源的细胞系KG-1和成骨肉瘤细胞系SaOS-2中发现了例外情况,以及在先前报道的EBV转化的B细胞系Wa中也有例外。为了确定这些受体的生化性质,对Wa细胞进行细胞表面生物素化,并通过免疫沉淀分离前S结合受体。在SDS-聚丙烯酰胺凝胶中鉴定出一条分子量约为30 kDa的特异性条带,对其进一步表征有望为HBV在肝细胞和肝外细胞中的感染机制提供线索。

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