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SARS-CoV-2 spike protein: structure, viral entry and variants.

作者信息

Chen Bing, Farzan Michael, Choe Hyeryun

机构信息

Division of Molecular Medicine, Boston Children's Hospital, and Department of Paediatrics, Harvard Medical School, Boston, MA, USA.

Division of Infectious Diseases, Boston Children's Hospital, and Department of Paediatrics, Harvard Medical School, Boston, MA, USA.

出版信息

Nat Rev Microbiol. 2025 May 6. doi: 10.1038/s41579-025-01185-8.


DOI:10.1038/s41579-025-01185-8
PMID:40328900
Abstract

Coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has been a devastating global pandemic for 4 years and is now an endemic disease. With the emergence of new viral variants, COVID-19 is a continuing threat to public health despite the wide availability of vaccines. The virus-encoded trimeric spike protein (S protein) mediates SARS-CoV-2 entry into host cells and also induces strong immune responses, making it an important target for development of therapeutics and vaccines. In this Review, we summarize our latest understanding of the structure and function of the SARS-CoV-2 S protein, the molecular mechanism of viral entry and the emergence of new variants, and we discuss their implications for development of S protein-related intervention strategies.

摘要

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引用本文的文献

[1]
Epitope Profiling of SARS-CoV-2 Spike Antigen Provides a Novel Strategy for Developing ELISAs Specific for Different Spike Protein Variants in Bivalent Vaccine Formulations.

Vaccines (Basel). 2025-7-26

[2]
Multiorgan Involvement and Particularly Liver Injury in Long COVID: A Narrative Review.

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本文引用的文献

[1]
Early fusion intermediate of ACE2-using coronavirus spike acting as an antiviral target.

Cell. 2025-3-6

[2]
Structural Immunology of SARS-CoV-2.

Immunol Rev. 2025-1

[3]
Design of customized coronavirus receptors.

Nature. 2024-11

[4]
Lineage-specific pathogenicity, immune evasion, and virological features of SARS-CoV-2 BA.2.86/JN.1 and EG.5.1/HK.3.

Nat Commun. 2024-10-9

[5]
Immune escape and attenuated severity associated with the SARS-CoV-2 BA.2.86/JN.1 lineage.

Nat Commun. 2024-10-3

[6]
Deep mutational scanning of SARS-CoV-2 Omicron BA.2.86 and epistatic emergence of the KP.3 variant.

Virus Evol. 2024-9-2

[7]
Genetic tracing of market wildlife and viruses at the epicenter of the COVID-19 pandemic.

Cell. 2024-9-19

[8]
Recurrent SARS-CoV-2 spike mutations confer growth advantages to select JN.1 sublineages.

Emerg Microbes Infect. 2024-12

[9]
Structural basis for the evolution and antibody evasion of SARS-CoV-2 BA.2.86 and JN.1 subvariants.

Nat Commun. 2024-9-4

[10]
Structure and inhibition of SARS-CoV-2 spike refolding in membranes.

Science. 2024-8-16

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