首页> 外文期刊>Cell structure and function >Identification of Fusion Regulatory Protein (FRP)-1/4F2 Related Molecules : Cytoskeletal Proteins are Associated with FRP-1 Molecules that Regulate Multinucleated Giant Cell Formation of Monocytes and HIV-Induced Cell Fusion
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Identification of Fusion Regulatory Protein (FRP)-1/4F2 Related Molecules : Cytoskeletal Proteins are Associated with FRP-1 Molecules that Regulate Multinucleated Giant Cell Formation of Monocytes and HIV-Induced Cell Fusion

机译:融合调节蛋白(FRP)-1 / 4F2相关分子的鉴定:细胞骨架蛋白与调节单核细胞多核巨细胞形成和HIV诱导的细胞融合的FRP-1分子相关。

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References(29) Cited-By(7) Fusion regulatory proteins (FRPs) regulate virus-mediated cell fusion and multinucleated giant cell formation of monocytes. Anti-FRP-1 mAbs immunoprecipitated 80 kDa and 38 kDa proteins from HeLa cells. After long exposure other bands were detected, suggesting the presence of molecule(s) associated with FRP-1. To identify the molecule(s), we prepared monoclonal antibodies against immunoaffinity-purified FRP-1 complex derived from membrane fractions of HeLa cells. Immunofluorescence microscopy revealed that these monoclonal antibodies recognized the intracytoplasmic molecules in HeLa cells. Using immunoblotting, the antibodies reacted with 200 kDa, 70 kDa, 55 kDa and 35 kDa molecules, so we designated these molecules as FRP related molecules (FRMs). Subsequently, we performed gene cloning from a HeLa λgt11 cDNA library using anti-FRM mAbs and immunoblotting analysis with either purified cytoskeletal proteins or specific antibodies against various cytoskeletal proteins. Three kinds of positive clone were obtained, which encoded partial sequences of vimentin, tropomyosin, and heat shock cognate protein 70 (hsc70). The 200 kDa molecule was expected to be a myosin heavy chain, judging from the immunoblotting pattern. Immunoblotting confirmed that these purified proteins were readily recognized by anti-FRM mAbs. Furthermore, anti-vimentin and anti-myosin mAbs reacted with the precipitates by anti-FRP-1 mAb, indicating a physical association between FRP-1 molecules and these cytoskeletal proteins. Whenanti-FRP-1 mAb was added to culture fluids of HeLa cells, the cell-shape and immunofluorescence-pattern stained with anti-FRM mAbs changed. Taken together, the fusion regulatory molecular complex is suggested to consist of at least FRP-1, hsc70, actomyosin and vimentin systems.
机译:参考文献(29)被引用的(7)融合调节蛋白(FRP)调节病毒介导的细胞融合和单核细胞的多核巨细胞形成。抗FRP-1 mAb可从HeLa细胞中免疫沉淀80 kDa和38 kDa蛋白。长时间暴露后,检测到其他条带,表明存在与FRP-1相关的分子。为了鉴定该分子,我们制备了针对源自HeLa细胞膜级分的免疫亲和纯化FRP-1复合物的单克隆抗体。免疫荧光显微镜检查显示,这些单克隆抗体识别HeLa细胞中的胞浆内分子。使用免疫印迹,抗体与200 kDa,70 kDa,55 kDa和35 kDa分子反应,因此我们将这些分子指定为FRP相关分子(FRM)。随后,我们使用抗FRM mAb从HeLaλgt11cDNA文库进行了基因克隆,并使用纯化的细胞骨架蛋白或针对各种细胞骨架蛋白的特异性抗体进行了免疫印迹分析。获得了三种阳性克隆,它们编码波形蛋白,原肌球蛋白和热休克同源蛋白70(hsc70)的部分序列。从免疫印迹模式来看,预计200 kDa分子是肌球蛋白重链。免疫印迹证实,这些纯化的蛋白质易于被抗FRM mAb识别。此外,抗波形蛋白和抗肌球蛋白单克隆抗体通过抗FRP-1 mAb与沉淀物反应,表明FRP-1分子与这些细胞骨架蛋白之间存在物理联系。当将抗FRP-1 mAb加入HeLa细胞的培养液中时,用抗FRM mAb染色的细胞形状和免疫荧光模式会发生变化。综上所述,融合调节分子复合物被建议至少由FRP-1,hsc70,放线菌素和波形蛋白系统组成。

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