首页> 外文期刊>Virology >Zhu, Y.-Z., Luo, Y., Cao, M.-M., Liu, Y., Liu, X.-Q., Wang, W., Wu, D.-G., Guan, M., Xu, Q.-Q., Ren, H., Zhao, P., Qi, Z.-T.Significance of palmitoylation of CD81 on its association with tetraspanin-enriched microdomains and mediating hepatitis C virus cell entry
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Zhu, Y.-Z., Luo, Y., Cao, M.-M., Liu, Y., Liu, X.-Q., Wang, W., Wu, D.-G., Guan, M., Xu, Q.-Q., Ren, H., Zhao, P., Qi, Z.-T.Significance of palmitoylation of CD81 on its association with tetraspanin-enriched microdomains and mediating hepatitis C virus cell entry

机译:朱艳珠,罗艳霞,曹明美,刘艳霞,刘新奇,王文武,吴德庚,关明徐Q-Q。任H.赵P.齐Z-T.CD81的棕榈酰化及其与富含四跨素的微结构域和介导丙型肝炎病毒细胞进入的关系

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摘要

CD81, a co-receptor for hepatitis C virus (HCV), is a member of the tetraspanin superfamily and is heavily palmitoylated in the juxtamembrane cysteine residues. Palmitoylation plays an important role in protein-protein interactions and association with cholesterol-rich domains of membranes. In this study, Huh7 cells expressing wild-type or palmitoylation-defective CD81 were generated to analyze whether palmitoylation of CD81 is involved in HCV cell entry. Our data showed that de-palmitoylation of CD81 dramatically reduced its association with tetraspanin CD151, but did not influence CD81 partition in detergent-resistant membranes. Moreover, de-palmitoylated CD81 decreased the host cell susceptibility to HCV. Notably, CD151-specific antibodies and siRNA inhibited HCV cell entry, and detachment of CD81 with CD151 decreased the lateral movement of virus particle/CD81 complex to areas of cell-cell contact. These results suggest that palmitoylation of CD81 should facilitate HCV entry, at least in part, by regulating the association of CD81 with tetraspanin-enriched microdomains.
机译:CD81是丙型肝炎病毒(HCV)的共同受体,是四跨素超家族的成员,在近膜半胱氨酸残基中被严重棕榈酰化。棕榈酰化在蛋白质与蛋白质的相互作用以及与富含胆固醇的膜结构域的结合中起着重要作用。在这项研究中,表达野生型或棕榈酰化缺陷型CD81的Huh7细胞被生成,以分析CD81的棕榈酰化是否参与HCV细胞进入。我们的数据表明,CD81的去棕榈酸酯化作用显着降低了它与四跨素CD151的缔合,但不影响耐洗涤剂膜中CD81的分配。而且,去棕榈酰化的CD81降低了宿主细胞对HCV的敏感性。值得注意的是,CD151特异性抗体和siRNA抑制了HCV细胞进入,而CD81与CD151的分离减少了病毒颗粒/ CD81复合物向细胞与细胞接触区域的横向移动。这些结果表明,CD81的棕榈酰化应至少部分地通过调节CD81与富含四跨膜蛋白的微结构域的缔合而促进HCV的进入。

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