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HIV-1包膜V3环裂解在细胞嗜性中的作用。

Role of HIV-1 envelope V3 loop cleavage in cell tropism.

作者信息

Gu R, Westervelt P, Ratner L

机构信息

Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.

出版信息

AIDS Res Hum Retroviruses. 1993 Oct;9(10):1007-15. doi: 10.1089/aid.1993.9.1007.

Abstract

The envelope protein is an important determinant of HIV-1 cell-specific tropism. The gp160 envelope precursor proteins from macrophage-tropic or T lymphoid cell line-tropic strains of HIV-1 were expressed in recombinant vaccinia virus-infected cell lines or primary lymphocytes or macrophages. No significant differences in the kinetics of synthesis of gp160, processing into gp120 and gp41 proteins, N-linked glycosylation, or release of gp120 into the medium were noted with the different envelope proteins. However, gp120 envelope protein shed into the medium was found to be at least partially cleaved at a site within the V3 loop. The gp120 envelope proteins from macrophage-tropic isolates exhibited lower rates of cleavage than those from lymphoid cell line-tropic strains in all cell types examined. Cell-free protease digestion studies also demonstrated relative resistance of the envelopes from macrophage-tropic compared to lymphoid cell line-tropic strains. All recombinant envelope proteins were recognized by monoclonal antibodies directed at gp41 or the C-terminal gp120 epitopes, and no differences in binding to CD4 were noted.

摘要

包膜蛋白是HIV-1细胞特异性嗜性的重要决定因素。来自HIV-1巨噬细胞嗜性或T淋巴细胞系嗜性毒株的gp160包膜前体蛋白在重组痘苗病毒感染的细胞系、原代淋巴细胞或巨噬细胞中表达。不同的包膜蛋白在gp160的合成动力学、加工成gp120和gp41蛋白、N-连接糖基化或gp120释放到培养基中的过程中未发现显著差异。然而,发现释放到培养基中的gp120包膜蛋白在V3环内的一个位点至少部分被切割。在所有检测的细胞类型中,来自巨噬细胞嗜性分离株的gp120包膜蛋白的切割率低于来自淋巴细胞系嗜性毒株的gp120包膜蛋白。无细胞蛋白酶消化研究也表明,与淋巴细胞系嗜性毒株相比,巨噬细胞嗜性毒株的包膜具有相对抗性。所有重组包膜蛋白都被针对gp41或gp120 C末端表位的单克隆抗体识别,并且在与CD4结合方面未发现差异。

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