Suppr超能文献

麻疹病毒附着蛋白的一系列构象变化启动了膜融合过程。

Sequential conformational changes in the morbillivirus attachment protein initiate the membrane fusion process.

作者信息

Ader-Ebert Nadine, Khosravi Mojtaba, Herren Michael, Avila Mislay, Alves Lisa, Bringolf Fanny, Örvell Claes, Langedijk Johannes P, Zurbriggen Andreas, Plemper Richard K, Plattet Philippe

机构信息

Division of Neurological Sciences, Department of Clinical Research and Veterinary Public Health (DCR-VPH), Vetsuisse Faculty, University of Bern, Bern, Switzerland; Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.

Division of Laboratory Medicine, Karolinska University Hospital Huddinge, Stockholm, Sweden.

出版信息

PLoS Pathog. 2015 May 6;11(5):e1004880. doi: 10.1371/journal.ppat.1004880. eCollection 2015 May.

Abstract

Despite large vaccination campaigns, measles virus (MeV) and canine distemper virus (CDV) cause major morbidity and mortality in humans and animals, respectively. The MeV and CDV cell entry system relies on two interacting envelope glycoproteins: the attachment protein (H), consisting of stalk and head domains, co-operates with the fusion protein (F) to mediate membrane fusion. However, how receptor-binding by the H-protein leads to F-triggering is not fully understood. Here, we report that an anti-CDV-H monoclonal antibody (mAb-1347), which targets the linear H-stalk segment 126-133, potently inhibits membrane fusion without interfering with H receptor-binding or F-interaction. Rather, mAb-1347 blocked the F-triggering function of H-proteins regardless of the presence or absence of the head domains. Remarkably, mAb-1347 binding to headless CDV H, as well as standard and engineered bioactive stalk-elongated CDV H-constructs treated with cells expressing the SLAM receptor, was enhanced. Despite proper cell surface expression, fusion promotion by most H-stalk mutants harboring alanine substitutions in the 126-138 "spacer" section was substantially impaired, consistent with deficient receptor-induced mAb-1347 binding enhancement. However, a previously reported F-triggering defective H-I98A variant still exhibited the receptor-induced "head-stalk" rearrangement. Collectively, our data spotlight a distinct mechanism for morbillivirus membrane fusion activation: prior to receptor contact, at least one of the morbillivirus H-head domains interacts with the membrane-distal "spacer" domain in the H-stalk, leaving the F-binding site located further membrane-proximal in the stalk fully accessible. This "head-to-spacer" interaction conformationally stabilizes H in an auto-repressed state, which enables intracellular H-stalk/F engagement while preventing the inherent H-stalk's bioactivity that may prematurely activate F. Receptor-contact disrupts the "head-to-spacer" interaction, which subsequently "unlocks" the stalk, allowing it to rearrange and trigger F. Overall, our study reveals essential mechanistic requirements governing the activation of the morbillivirus membrane fusion cascade and spotlights the H-stalk "spacer" microdomain as a possible drug target for antiviral therapy.

摘要

尽管开展了大规模疫苗接种运动,但麻疹病毒(MeV)和犬瘟热病毒(CDV)分别在人类和动物中导致了严重的发病和死亡。MeV和CDV的细胞进入系统依赖于两种相互作用的包膜糖蛋白:附着蛋白(H),由茎部和头部结构域组成,与融合蛋白(F)协同介导膜融合。然而,H蛋白与受体的结合如何导致F的触发尚未完全了解。在这里,我们报告一种靶向线性H茎段126 - 133的抗CDV - H单克隆抗体(mAb - 1347),能有效抑制膜融合,而不干扰H与受体的结合或F的相互作用。相反,无论头部结构域是否存在,mAb - 1347都能阻断H蛋白的F触发功能。值得注意的是,mAb - 1347与无头CDV H以及用表达信号淋巴细胞激活分子相关受体(SLAM)的细胞处理过的标准和工程化生物活性茎段延长的CDV H构建体的结合增强。尽管在细胞表面正确表达,但大多数在126 - 138“间隔区”带有丙氨酸取代的H茎突变体促进融合的能力显著受损,这与受体诱导的mAb - 1347结合增强缺陷一致。然而,先前报道的F触发缺陷型H - I98A变体仍表现出受体诱导的“头 -茎”重排。总体而言,我们的数据突出了麻疹病毒膜融合激活的一种独特机制:在受体接触之前,麻疹病毒H头部结构域中的至少一个与H茎中膜远端的“间隔区”结构域相互作用,使茎中更靠近膜近端的F结合位点完全可及。这种“头对间隔区”的相互作用在构象上使H稳定在一种自抑制状态,这使得细胞内H茎/F能够结合,同时防止了可能过早激活F的固有H茎的生物活性。受体接触破坏了“头对间隔区”的相互作用,随后“解锁”茎,使其能够重排并触发F。总的来说,我们的研究揭示了控制麻疹病毒膜融合级联激活的基本机制要求,并突出了H茎“间隔区”微结构域作为抗病毒治疗可能的药物靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aec7/4422687/2080cdbd0e02/ppat.1004880.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验