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2
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本文引用的文献

1
Comprehensive functional analysis of N-linked glycans on Ebola virus GP1.埃博拉病毒糖蛋白1(GP1)上N-连接聚糖的综合功能分析
mBio. 2014 Jan 28;5(1):e00862-13. doi: 10.1128/mBio.00862-13.
2
Multiple cationic amphiphiles induce a Niemann-Pick C phenotype and inhibit Ebola virus entry and infection.多种阳离子两亲化合物诱导尼曼-匹克 C 型表型并抑制埃博拉病毒进入和感染。
PLoS One. 2013;8(2):e56265. doi: 10.1371/journal.pone.0056265. Epub 2013 Feb 18.
3
Delayed treatment of Ebola virus infection with plant-derived monoclonal antibodies provides protection in rhesus macaques.植物源单克隆抗体延迟埃博拉病毒感染治疗可为恒河猴提供保护。
Proc Natl Acad Sci U S A. 2012 Oct 30;109(44):18030-5. doi: 10.1073/pnas.1213709109. Epub 2012 Oct 15.
4
Structural mechanism of trimeric HIV-1 envelope glycoprotein activation.三聚体 HIV-1 包膜糖蛋白激活的结构机制。
PLoS Pathog. 2012;8(7):e1002797. doi: 10.1371/journal.ppat.1002797. Epub 2012 Jul 12.
5
Successful treatment of ebola virus-infected cynomolgus macaques with monoclonal antibodies.用单克隆抗体成功治疗感染埃博拉病毒的食蟹猴。
Sci Transl Med. 2012 Jun 13;4(138):138ra81. doi: 10.1126/scitranslmed.3003876.
6
Ebola virus entry requires the host-programmed recognition of an intracellular receptor.埃博拉病毒进入宿主需要宿主程序化识别细胞内受体。
EMBO J. 2012 Apr 18;31(8):1947-60. doi: 10.1038/emboj.2012.53. Epub 2012 Mar 6.
7
The organisation of Ebola virus reveals a capacity for extensive, modular polyploidy.埃博拉病毒的组织方式揭示了其具有广泛的、模块化的多倍体能力。
PLoS One. 2012;7(1):e29608. doi: 10.1371/journal.pone.0029608. Epub 2012 Jan 11.
8
Structure of an antibody in complex with its mucin domain linear epitope that is protective against Ebola virus.与保护性埃博拉病毒抗体结合的粘蛋白域线性表位的结构。
J Virol. 2012 Mar;86(5):2809-16. doi: 10.1128/JVI.05549-11. Epub 2011 Dec 14.
9
Impact of Ebola mucin-like domain on antiglycoprotein antibody responses induced by Ebola virus-like particles.埃博拉糖蛋白类似结构域对埃博拉病毒样颗粒诱导的抗糖蛋白抗体应答的影响。
J Infect Dis. 2011 Nov;204 Suppl 3(Suppl 3):S825-32. doi: 10.1093/infdis/jir295.
10
Molecular architectures of trimeric SIV and HIV-1 envelope glycoproteins on intact viruses: strain-dependent variation in quaternary structure.三聚体 SIV 和 HIV-1 包膜糖蛋白在完整病毒上的分子结构:四级结构的株系差异。
PLoS Pathog. 2010 Dec 23;6(12):e1001249. doi: 10.1371/journal.ppat.1001249.

通过冷冻电子断层扫描确定埃博拉病毒糖蛋白粘蛋白样结构域的空间定位。

Spatial localization of the Ebola virus glycoprotein mucin-like domain determined by cryo-electron tomography.

作者信息

Tran Erin E H, Simmons James A, Bartesaghi Alberto, Shoemaker Charles J, Nelson Elizabeth, White Judith M, Subramaniam Sriram

机构信息

Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.

Department of Cell Biology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.

出版信息

J Virol. 2014 Sep;88(18):10958-62. doi: 10.1128/JVI.00870-14. Epub 2014 Jul 9.

DOI:10.1128/JVI.00870-14
PMID:25008940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4178867/
Abstract

The Ebola virus glycoprotein mucin-like domain (MLD) is implicated in Ebola virus cell entry and immune evasion. Using cryo-electron tomography of Ebola virus-like particles, we determined a three-dimensional structure for the full-length glycoprotein in a near-native state and compared it to that of a glycoprotein lacking the MLD. Our results, which show that the MLD is located at the apex and the sides of each glycoprotein monomer, provide a structural template for analysis of MLD function.

摘要

埃博拉病毒糖蛋白粘蛋白样结构域(MLD)与埃博拉病毒进入细胞及免疫逃逸有关。通过对埃博拉病毒样颗粒进行冷冻电子断层扫描,我们确定了全长糖蛋白在近天然状态下的三维结构,并将其与缺乏MLD的糖蛋白结构进行比较。我们的结果表明,MLD位于每个糖蛋白单体的顶端和侧面,为分析MLD功能提供了结构模板。