• 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

冠状病毒与受体相互作用的结构观点。

A structural view of coronavirus-receptor interactions.

作者信息

Reguera Juan, Mudgal Gaurav, Santiago César, Casasnovas José M

机构信息

European Molecular Biology Laboratory, Grenoble Outstation, Grenoble Cedex 9, France.

Centro Nacional de Biotecnología (CNB-CSIC), Campus Universidad Autónoma, Darwin 3, 28049 Madrid, Spain.

出版信息

Virus Res. 2014 Dec 19;194:3-15. doi: 10.1016/j.virusres.2014.10.005. Epub 2014 Oct 14.

DOI:10.1016/j.virusres.2014.10.005
PMID:25451063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7114462/
Abstract

In the coronavirus (CoV), the envelope spike (S) glycoprotein is responsible for CoV cell entry and host-to-host transmission. The S is a multifunctional glycoprotein that mediates both attachment of CoV particles to cell surface receptor molecules as well as membrane penetration by fusion. Receptor-binding domains (RBD) have been identified in the S of diverse CoV; they usually contain antigenic determinants targeted by antibodies that neutralize CoV infections. To penetrate host cells, the CoV can use various cell surface molecules, although they preferentially bind to ectoenzymes. Several crystal structures have determined the folding of CoV RBD and the mode by which they recognize cell entry receptors. Here we review the CoV-receptor complex structures reported to date, and highlight the distinct receptor recognition modes, common features, and key determinants of the binding specificity. Structural studies have established the basis for understanding receptor recognition diversity in CoV, its evolution and the adaptation of this virus family to different hosts. CoV responsible for recent outbreaks have extraordinary potential for cross-species transmission; their RBD bear large platforms specialized in recognition of receptors from different species, which facilitates host-to-host circulation and adaptation to man.

摘要

在冠状病毒(CoV)中,包膜刺突(S)糖蛋白负责CoV进入细胞以及在宿主之间传播。S是一种多功能糖蛋白,它介导CoV颗粒与细胞表面受体分子的结合以及通过融合实现膜穿透。在多种CoV的S蛋白中已鉴定出受体结合域(RBD);它们通常包含被中和CoV感染的抗体靶向的抗原决定簇。为了穿透宿主细胞,CoV可以利用各种细胞表面分子,尽管它们优先结合胞外酶。几种晶体结构已经确定了CoV RBD的折叠方式及其识别细胞进入受体的模式。在这里,我们综述了迄今为止报道的CoV-受体复合物结构,并强调了不同的受体识别模式、共同特征以及结合特异性的关键决定因素。结构研究为理解CoV中受体识别的多样性、其进化以及该病毒家族对不同宿主的适应性奠定了基础。导致近期疫情爆发的CoV具有跨物种传播的巨大潜力;它们的RBD具有专门用于识别来自不同物种受体的大平台,这有利于在宿主之间传播并适应人类。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/8f673bcba7ec/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/634db20d592b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/f91aa962f700/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/35f3bafd50a5/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/c99ff6e778dd/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/196fa4795668/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/fabf47ce0781/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/ebd72b22232a/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/50844346b15e/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/4e7237030816/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/8f673bcba7ec/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/634db20d592b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/f91aa962f700/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/35f3bafd50a5/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/c99ff6e778dd/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/196fa4795668/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/fabf47ce0781/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/ebd72b22232a/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/50844346b15e/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/4e7237030816/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5af/7114462/8f673bcba7ec/gr10.jpg

相似文献

1
A structural view of coronavirus-receptor interactions.冠状病毒与受体相互作用的结构观点。
Virus Res. 2014 Dec 19;194:3-15. doi: 10.1016/j.virusres.2014.10.005. Epub 2014 Oct 14.
2
Spread of Mutant Middle East Respiratory Syndrome Coronavirus with Reduced Affinity to Human CD26 during the South Korean Outbreak.韩国疫情期间对人CD26亲和力降低的中东呼吸综合征冠状病毒突变株的传播
mBio. 2016 Mar 1;7(2):e00019. doi: 10.1128/mBio.00019-16.
3
Identification of the Receptor-Binding Domain of the Spike Glycoprotein of Human Betacoronavirus HKU1.人乙型冠状病毒HKU1刺突糖蛋白受体结合域的鉴定
J Virol. 2015 Sep;89(17):8816-27. doi: 10.1128/JVI.03737-14. Epub 2015 Jun 17.
4
Putative Receptor Binding Domain of Bat-Derived Coronavirus HKU9 Spike Protein: Evolution of Betacoronavirus Receptor Binding Motifs.蝙蝠源冠状病毒HKU9刺突蛋白的假定受体结合域:β冠状病毒受体结合基序的进化
Biochemistry. 2016 Nov 1;55(43):5977-5988. doi: 10.1021/acs.biochem.6b00790. Epub 2016 Oct 18.
5
Recombinant Receptor-Binding Domains of Multiple Middle East Respiratory Syndrome Coronaviruses (MERS-CoVs) Induce Cross-Neutralizing Antibodies against Divergent Human and Camel MERS-CoVs and Antibody Escape Mutants.多种中东呼吸综合征冠状病毒(MERS-CoV)的重组受体结合结构域可诱导产生针对不同人类和骆驼MERS-CoV以及抗体逃逸突变体的交叉中和抗体。
J Virol. 2016 Dec 16;91(1). doi: 10.1128/JVI.01651-16. Print 2017 Jan 1.
6
Identification of sialic acid-binding function for the Middle East respiratory syndrome coronavirus spike glycoprotein.鉴定中东呼吸综合征冠状病毒刺突糖蛋白的唾液酸结合功能。
Proc Natl Acad Sci U S A. 2017 Oct 3;114(40):E8508-E8517. doi: 10.1073/pnas.1712592114. Epub 2017 Sep 18.
7
Crystallization and Structural Determination of the Receptor-Binding Domain of MERS-CoV Spike Glycoprotein.中东呼吸综合征冠状病毒刺突糖蛋白受体结合结构域的结晶与结构测定
Methods Mol Biol. 2020;2099:39-50. doi: 10.1007/978-1-0716-0211-9_4.
8
Mutations in the Spike Protein of Middle East Respiratory Syndrome Coronavirus Transmitted in Korea Increase Resistance to Antibody-Mediated Neutralization.韩国传播的中东呼吸综合征冠状病毒刺突蛋白突变增加了对抗体介导的中和作用的抵抗力。
J Virol. 2019 Jan 4;93(2). doi: 10.1128/JVI.01381-18. Print 2019 Jan 15.
9
Structure of mouse coronavirus spike protein complexed with receptor reveals mechanism for viral entry.鼠冠状病毒刺突蛋白复合物与受体的结构揭示了病毒进入的机制。
PLoS Pathog. 2020 Mar 9;16(3):e1008392. doi: 10.1371/journal.ppat.1008392. eCollection 2020 Mar.
10
Research progress on coronavirus S proteins and their receptors.冠状病毒 S 蛋白及其受体的研究进展。
Arch Virol. 2021 Jul;166(7):1811-1817. doi: 10.1007/s00705-021-05008-y. Epub 2021 Mar 28.

引用本文的文献

1
Assessment for Risk of Possible Human Transmission of FCoV-23.评估猫冠状病毒23型可能发生人际传播的风险。
Transbound Emerg Dis. 2024 Oct 1;2024:8398470. doi: 10.1155/2024/8398470. eCollection 2024.
2
Virus-Receptor Interactions and Receptor-Mediated Virus Entry into Host Cells.病毒-受体相互作用以及受体介导的病毒进入宿主细胞
Subcell Biochem. 2024;105:533-566. doi: 10.1007/978-3-031-65187-8_15.
3
A Genetically Engineered Bivalent Vaccine Coexpressing a Molecular Adjuvant against Classical Swine Fever and Porcine Epidemic Diarrhea.

本文引用的文献

1
Bat origins of MERS-CoV supported by bat coronavirus HKU4 usage of human receptor CD26.蝙蝠冠状病毒HKU4对人类受体CD26的利用支持中东呼吸综合征冠状病毒起源于蝙蝠。
Cell Host Microbe. 2014 Sep 10;16(3):328-37. doi: 10.1016/j.chom.2014.08.009.
2
Receptor usage and cell entry of bat coronavirus HKU4 provide insight into bat-to-human transmission of MERS coronavirus.蝙蝠冠状病毒HKU4的受体使用情况及细胞进入机制为中东呼吸综合征冠状病毒从蝙蝠向人类的传播提供了线索。
Proc Natl Acad Sci U S A. 2014 Aug 26;111(34):12516-21. doi: 10.1073/pnas.1405889111. Epub 2014 Aug 11.
3
Host species restriction of Middle East respiratory syndrome coronavirus through its receptor, dipeptidyl peptidase 4.
一种表达针对经典猪瘟和猪流行性腹泻的分子佐剂的基因工程二价疫苗。
Int J Mol Sci. 2023 Jul 26;24(15):11954. doi: 10.3390/ijms241511954.
4
Significance of Conserved Regions in Coronavirus Spike Protein for Developing a Novel Vaccine against SARS-CoV-2 Infection.冠状病毒刺突蛋白中保守区域对研发抗SARS-CoV-2感染新型疫苗的意义
Vaccines (Basel). 2023 Feb 24;11(3):545. doi: 10.3390/vaccines11030545.
5
Physico-Chemical Mechanisms of the Functioning of Membrane-Active Proteins of Enveloped Viruses.包膜病毒膜活性蛋白功能的物理化学机制
Biochem (Mosc) Suppl Ser A Membr Cell Biol. 2022;16(4):247-260. doi: 10.1134/S1990747822050038. Epub 2022 Dec 9.
6
DNAJA3 Interacts with PEDV S1 Protein and Inhibits Virus Replication by Affecting Virus Adsorption to Host Cells.DNAJA3 与 PEDV S1 蛋白相互作用,通过影响病毒吸附到宿主细胞来抑制病毒复制。
Viruses. 2022 Oct 31;14(11):2413. doi: 10.3390/v14112413.
7
SARS-CoV-2 spike protein detection using slightly tapered no-core fiber-based optical transducer.基于稍有锥形无芯光纤的光学换能器检测 SARS-CoV-2 刺突蛋白。
Mikrochim Acta. 2022 Aug 6;189(9):321. doi: 10.1007/s00604-022-05413-3.
8
Coronavirus as a Trigger Of Graves' Disease.冠状病毒作为格雷夫斯病的诱因
Acta Endocrinol (Buchar). 2021 Jul-Sep;17(3):413-415. doi: 10.4183/aeb.2021.413.
9
Conserved Targets to Prevent Emerging Coronaviruses.预防新型冠状病毒的保守靶点。
Viruses. 2022 Mar 9;14(3):563. doi: 10.3390/v14030563.
10
Known Cellular and Receptor Interactions of Animal and Human Coronaviruses: A Review.已知的动物和人类冠状病毒的细胞和受体相互作用:综述。
Viruses. 2022 Feb 8;14(2):351. doi: 10.3390/v14020351.
通过其受体二肽基肽酶 4 限制中东呼吸综合征冠状病毒的宿主物种。
J Virol. 2014 Aug;88(16):9220-32. doi: 10.1128/JVI.00676-14. Epub 2014 Jun 4.
4
Coronaviruses: important emerging human pathogens.冠状病毒:重要的新兴人类病原体。
J Virol. 2014 May;88(10):5209-12. doi: 10.1128/JVI.03488-13. Epub 2014 Mar 5.
5
MERS: emergence of a novel human coronavirus.中东呼吸综合征冠状病毒(MERS-CoV):一种新型人类冠状病毒的出现。
Curr Opin Virol. 2014 Apr;5:58-62. doi: 10.1016/j.coviro.2014.01.010. Epub 2014 Feb 28.
6
Middle East respiratory syndrome coronavirus in dromedary camels: an outbreak investigation.中东呼吸综合征冠状病毒在单峰驼中的流行情况:暴发调查。
Lancet Infect Dis. 2014 Feb;14(2):140-5. doi: 10.1016/S1473-3099(13)70690-X. Epub 2013 Dec 17.
7
Receptor recognition and cross-species infections of SARS coronavirus.SARS 冠状病毒的受体识别和跨种感染。
Antiviral Res. 2013 Oct;100(1):246-54. doi: 10.1016/j.antiviral.2013.08.014. Epub 2013 Aug 29.
8
Crystal structure of the receptor-binding domain from newly emerged Middle East respiratory syndrome coronavirus.新型中东呼吸综合征冠状病毒受体结合结构域的晶体结构
J Virol. 2013 Oct;87(19):10777-83. doi: 10.1128/JVI.01756-13. Epub 2013 Jul 31.
9
Structure of MERS-CoV spike receptor-binding domain complexed with human receptor DPP4.MERS-CoV 刺突受体结合域与人受体 DPP4 复合物的结构。
Cell Res. 2013 Aug;23(8):986-93. doi: 10.1038/cr.2013.92. Epub 2013 Jul 9.
10
Molecular basis of binding between novel human coronavirus MERS-CoV and its receptor CD26.新型人类冠状病毒 MERS-CoV 与其受体 CD26 结合的分子基础。
Nature. 2013 Aug 8;500(7461):227-31. doi: 10.1038/nature12328. Epub 2013 Jul 7.