• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

登革病毒糖基化:我们了解多少?

Dengue Virus Glycosylation: What Do We Know?

作者信息

Yap Sally S L, Nguyen-Khuong Terry, Rudd Pauline M, Alonso Sylvie

机构信息

Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, and Immunology program, Life Sciences Institute, National University of SingaporeSingapore, Singapore.

Analytics Group, Bioprocessing Technology Institute, A∗STARSingapore, Singapore.

出版信息

Front Microbiol. 2017 Jul 25;8:1415. doi: 10.3389/fmicb.2017.01415. eCollection 2017.

DOI:10.3389/fmicb.2017.01415
PMID:28791003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5524768/
Abstract

In many infectious diseases caused by either viruses or bacteria, pathogen glycoproteins play important roles during the infection cycle, ranging from entry to successful intracellular replication and host immune evasion. Dengue is no exception. glycoproteins, envelope protein (E) and non-structural protein 1 (NS1) are two popular sub-unit vaccine candidates. E protein on the virion surface is the major target of neutralizing antibodies. NS1 which is secreted during DENV infection has been shown to induce a variety of host responses through its binding to several host factors. However, despite their critical role in disease and protection, the glycosylated variants of these two proteins and their biological importance have remained understudied. In this review, we seek to provide a comprehensive summary of the current knowledge on protein glycosylation in DENV, and its role in virus biogenesis, host cell receptor interaction and disease pathogenesis.

摘要

在许多由病毒或细菌引起的传染病中,病原体糖蛋白在感染周期中发挥着重要作用,从进入宿主细胞到成功进行细胞内复制以及逃避宿主免疫。登革热也不例外。糖蛋白、包膜蛋白(E)和非结构蛋白1(NS1)是两种常见的亚单位疫苗候选物。病毒粒子表面的E蛋白是中和抗体的主要靶标。登革病毒感染期间分泌的NS1已被证明通过与多种宿主因子结合诱导多种宿主反应。然而,尽管它们在疾病和保护中起着关键作用,但这两种蛋白的糖基化变体及其生物学重要性仍未得到充分研究。在本综述中,我们试图全面总结目前关于登革病毒中蛋白质糖基化的知识,及其在病毒生物发生、宿主细胞受体相互作用和疾病发病机制中的作用。

相似文献

1
Dengue Virus Glycosylation: What Do We Know?登革病毒糖基化:我们了解多少?
Front Microbiol. 2017 Jul 25;8:1415. doi: 10.3389/fmicb.2017.01415. eCollection 2017.
2
Dengue Virus Non-structural Protein 1 Modulates Infectious Particle Production via Interaction with the Structural Proteins.登革病毒非结构蛋白1通过与结构蛋白相互作用调节感染性颗粒的产生。
PLoS Pathog. 2015 Nov 12;11(11):e1005277. doi: 10.1371/journal.ppat.1005277. eCollection 2015.
3
Virus-like particles derived from Pichia pastoris-expressed dengue virus type 1 glycoprotein elicit homotypic virus-neutralizing envelope domain III-directed antibodies.源自毕赤酵母表达的1型登革病毒糖蛋白的病毒样颗粒可引发同型病毒中和性包膜结构域III导向抗体。
BMC Biotechnol. 2016 Jun 14;16(1):50. doi: 10.1186/s12896-016-0280-y.
4
Human glucose-regulated protein 78 modulates intracellular production and secretion of nonstructural protein 1 of dengue virus.人葡萄糖调节蛋白 78 调节登革病毒非结构蛋白 1 的细胞内产生和分泌。
J Gen Virol. 2018 Oct;99(10):1391-1406. doi: 10.1099/jgv.0.001134. Epub 2018 Aug 10.
5
A Global Interactome Map of the Dengue Virus NS1 Identifies Virus Restriction and Dependency Host Factors.登革热病毒 NS1 的全球相互作用组图谱鉴定出了病毒限制和宿主依赖性因子。
Cell Rep. 2017 Dec 26;21(13):3900-3913. doi: 10.1016/j.celrep.2017.11.094.
6
The Good, the Bad, and the Shocking: The Multiple Roles of Dengue Virus Nonstructural Protein 1 in Protection and Pathogenesis.好、坏、惊:登革病毒非结构蛋白 1 在保护和发病机制中的多重作用。
Annu Rev Virol. 2018 Sep 29;5(1):227-253. doi: 10.1146/annurev-virology-101416-041848. Epub 2018 Jul 25.
7
Mass spectrometric analysis of host cell proteins interacting with dengue virus nonstructural protein 1 in dengue virus-infected HepG2 cells.登革病毒感染的HepG2细胞中与登革病毒非结构蛋白1相互作用的宿主细胞蛋白的质谱分析。
Biochim Biophys Acta. 2016 Sep;1864(9):1270-1280. doi: 10.1016/j.bbapap.2016.04.008. Epub 2016 Apr 21.
8
Antibody-Dependent Dengue Virus Entry Modulates Cell Intrinsic Responses for Enhanced Infection.抗体依赖性登革病毒进入调节细胞固有反应增强感染。
mSphere. 2019 Sep 18;4(5):e00528-19. doi: 10.1128/mSphere.00528-19.
9
Inhibition of the Membrane Attack Complex by Dengue Virus NS1 through Interaction with Vitronectin and Terminal Complement Proteins.登革病毒NS1通过与玻连蛋白和补体末端蛋白相互作用抑制膜攻击复合物
J Virol. 2016 Oct 14;90(21):9570-9581. doi: 10.1128/JVI.00912-16. Print 2016 Nov 1.
10
-Expressed Bivalent Virus-Like Particulate Vaccine Induces Domain III-Focused Bivalent Neutralizing Antibodies without Antibody-Dependent Enhancement .表达的二价病毒样颗粒疫苗诱导以结构域III为靶点的二价中和抗体,且无抗体依赖增强作用。
Front Microbiol. 2018 Jan 9;8:2644. doi: 10.3389/fmicb.2017.02644. eCollection 2017.

引用本文的文献

1
Factors determining the outcomes of immune imprinting after repeated orthoflavivirus infections.决定反复感染黄病毒属病毒后免疫印记结果的因素。
Front Immunol. 2025 Jul 16;16:1560851. doi: 10.3389/fimmu.2025.1560851. eCollection 2025.
2
Overcoming dengue vaccine challenges through next-generation virus-like particle immunization strategies.通过下一代病毒样颗粒免疫策略克服登革热疫苗挑战。
Front Cell Infect Microbiol. 2025 Jun 16;15:1614805. doi: 10.3389/fcimb.2025.1614805. eCollection 2025.
3
Pathogenicity and virulence of Powassan virus.

本文引用的文献

1
Dengue Virus Infection Is through a Cooperative Interaction between a Mannose Receptor and CLEC5A on Macrophage as a Multivalent Hetero-Complex.登革病毒感染是通过巨噬细胞上的甘露糖受体和CLEC5A之间作为多价异源复合物的协同相互作用实现的。
PLoS One. 2016 Nov 10;11(11):e0166474. doi: 10.1371/journal.pone.0166474. eCollection 2016.
2
Hybrid mass spectrometry approaches in glycoprotein analysis and their usage in scoring biosimilarity.糖蛋白分析中的混合质谱方法及其在生物类似药评分中的应用。
Nat Commun. 2016 Nov 8;7:13397. doi: 10.1038/ncomms13397.
3
Secreted NS1 Protects Dengue Virus from Mannose-Binding Lectin-Mediated Neutralization.
波瓦桑病毒的致病性和毒力
Virulence. 2025 Dec;16(1):2523887. doi: 10.1080/21505594.2025.2523887. Epub 2025 Jun 26.
4
The hidden impact of producer cells on virion composition and infectivity.生产者细胞对病毒粒子组成和感染性的潜在影响。
Future Virol. 2025;20(3-4):113-123. doi: 10.1080/17460794.2025.2475669. Epub 2025 Mar 12.
5
Evolution and adaptation of dengue virus in response to high-temperature passaging in mosquito cells.登革病毒在蚊细胞中高温传代后的进化与适应性
Virus Evol. 2025 Apr 24;11(1):veaf016. doi: 10.1093/ve/veaf016. eCollection 2025.
6
The glycosylation deficiency of flavivirus NS1 attenuates virus replication through interfering with the formation of viral replication compartments.黄病毒 NS1 的糖基化缺陷通过干扰病毒复制隔间的形成来减弱病毒复制。
J Biomed Sci. 2024 Jun 7;31(1):60. doi: 10.1186/s12929-024-01048-z.
7
Dengue virus pathogenesis and host molecular machineries.登革病毒发病机制与宿主分子机制。
J Biomed Sci. 2024 Apr 22;31(1):43. doi: 10.1186/s12929-024-01030-9.
8
Alpha-mannosidase-2 modulates arbovirus infection in a pathogen- and Wolbachia-specific manner in Aedes aegypti mosquitoes.α-甘露糖苷酶-2 以病原体和沃尔巴克氏体特异性方式调节埃及伊蚊中虫媒病毒的感染。
Insect Mol Biol. 2024 Aug;33(4):362-371. doi: 10.1111/imb.12904. Epub 2024 Mar 7.
9
Antibody and Cell-Based Therapies against Virus-Induced Cancers in the Context of HIV/AIDS.在艾滋病毒/艾滋病背景下针对病毒诱导癌症的抗体和基于细胞的疗法。
Pathogens. 2023 Dec 22;13(1):14. doi: 10.3390/pathogens13010014.
10
-Specific Fitness Increase of Vesicular Stomatitis Virus in Insect-to-Insect Infections.-水疱性口炎病毒在昆虫间感染中的特异性适应性增强。
Insects. 2024 Jan 5;15(1):34. doi: 10.3390/insects15010034.
分泌型NS1蛋白可保护登革病毒免受甘露糖结合凝集素介导的中和作用。
J Immunol. 2016 Nov 15;197(10):4053-4065. doi: 10.4049/jimmunol.1600323. Epub 2016 Oct 19.
4
Site-Specific N- and O-Glycopeptide Analysis Using an Integrated C18-PGC-LC-ESI-QTOF-MS/MS Approach.使用集成的C18-PGC-LC-ESI-QTOF-MS/MS方法进行位点特异性N-糖肽和O-糖肽分析
Methods Mol Biol. 2017;1503:109-119. doi: 10.1007/978-1-4939-6493-2_9.
5
Glycan shield and epitope masking of a coronavirus spike protein observed by cryo-electron microscopy.通过冷冻电子显微镜观察到的冠状病毒刺突蛋白的聚糖屏蔽和表位掩盖
Nat Struct Mol Biol. 2016 Oct;23(10):899-905. doi: 10.1038/nsmb.3293. Epub 2016 Sep 12.
6
Complement in disease: a defence system turning offensive.补体系统在疾病中的作用:防御系统转为进攻。
Nat Rev Nephrol. 2016 Jul;12(7):383-401. doi: 10.1038/nrneph.2016.70. Epub 2016 May 23.
7
Iminosugars Inhibit Dengue Virus Production via Inhibition of ER Alpha-Glucosidases--Not Glycolipid Processing Enzymes.亚氨基糖通过抑制内质网α-葡萄糖苷酶而非糖脂加工酶来抑制登革病毒的产生。
PLoS Negl Trop Dis. 2016 Mar 14;10(3):e0004524. doi: 10.1371/journal.pntd.0004524. eCollection 2016 Mar.
8
Inhibition of endoplasmic reticulum glucosidases is required for in vitro and in vivo dengue antiviral activity by the iminosugar UV-4.抑制内质网葡萄糖苷酶是亚氨基糖UV-4在体外和体内产生登革热抗病毒活性所必需的。
Antiviral Res. 2016 May;129:93-98. doi: 10.1016/j.antiviral.2016.03.001. Epub 2016 Mar 3.
9
Maturing Glycoproteomics Technologies Provide Unique Structural Insights into the N-glycoproteome and Its Regulation in Health and Disease.成熟的糖蛋白质组学技术为N-糖蛋白质组及其在健康与疾病中的调控提供了独特的结构见解。
Mol Cell Proteomics. 2016 Jun;15(6):1773-90. doi: 10.1074/mcp.O115.057638. Epub 2016 Feb 29.
10
Challenges of glycosylation analysis and control: an integrated approach to producing optimal and consistent therapeutic drugs.糖基化分析与控制的挑战:生产优质且一致的治疗药物的综合方法。
Drug Discov Today. 2016 May;21(5):740-65. doi: 10.1016/j.drudis.2016.01.006. Epub 2016 Jan 25.