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首页> 外文期刊>FEMS Microbiology Letters >Relationships between the anti-HIV V-3-derived peptide SPC3 and lymphocyte membrane properties involved in virus entry: SPC3 interferes with CXCR4
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Relationships between the anti-HIV V-3-derived peptide SPC3 and lymphocyte membrane properties involved in virus entry: SPC3 interferes with CXCR4

机译:抗HIV V-3衍生肽SPC3与病毒进入涉及的淋巴细胞膜特性之间的关系:SPC3干扰CXCR4

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摘要

SPC3 is a multiple antigen peptide derived from the V-3 loop of human immunodeficiency virus (HIV) envelope (Env). II exerts a potent anti-HIV activity whereas it alters neither Env expression nor binding to CD4. Here, SPC3 binding characteristics, its subsequent intracellular fate and the fact that it inhibited SDF(1)alpha binding to the lymphocyte surface provided strong arguments to conclude that it exerts its anti-HIV activity through interference with the CXCR4 coreceptor. In contrast, it interferes with none of the other major surface proteins and mechanisms involving V-3 and implicated in infection, as shown here. This work identifies the target mechanism of SPC3. (C) 2000 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved. [References: 18]
机译:SPC3是一种多抗原肽,源自人免疫缺陷病毒(HIV)包膜(Env)的V-3环。 II具有强大的抗HIV活性,而它既不改变Env表达,也不改变与CD4的结合。在这里,SPC3的结合特性,其随后的细胞内命运以及它抑制SDF(1)alpha与淋巴细胞表面结合的事实提供了有力的论据,可以得出结论,其通过干扰CXCR4核心受体发挥其抗HIV活性。相反,它不干扰涉及V-3并与感染有关的其他主要表面蛋白和机制,如此处所示。这项工作确定了SPC3的目标机制。 (C)2000年欧洲微生物学会联合会。由Elsevier Science B.V.保留所有权利。 [参考:18]

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