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2
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Computational Alanine Scanning and Structural Analysis of the SARS-CoV-2 Spike Protein/Angiotensin-Converting Enzyme 2 Complex.基于 SARS-CoV-2 刺突蛋白/血管紧张素转化酶 2 复合物的丙氨酸扫描计算和结构分析。
ACS Nano. 2020 Sep 22;14(9):11821-11830. doi: 10.1021/acsnano.0c04674. Epub 2020 Aug 26.

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1
The Effect of Select SARS-CoV-2 N-Linked Glycan and Variant of Concern Spike Protein Mutations on C-Type Lectin-Receptor-Mediated Infection.SARS-CoV-2 N-连接聚糖和关注的 Spike 蛋白突变对 C 型凝集素受体介导感染的影响。
Viruses. 2023 Sep 9;15(9):1901. doi: 10.3390/v15091901.
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A special issue of IUBMB Life celebrating the 50th anniversary of FAOBMB (1972-2022).《国际生物化学与分子生物学联盟生活》特刊,庆祝国际生物化学与分子生物学联盟(FAOBMB)成立50周年(1972 - 2022)。
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本文引用的文献

1
O-Linked Sialoglycans Modulate the Proteolysis of SARS-CoV-2 Spike and Likely Contribute to the Mutational Trajectory in Variants of Concern.O-连接唾液酸聚糖调节严重急性呼吸综合征冠状病毒2刺突蛋白的蛋白水解作用,并可能促成关注变异株的突变轨迹。
ACS Cent Sci. 2023 Feb 16;9(3):393-404. doi: 10.1021/acscentsci.2c01349. eCollection 2023 Mar 22.
2
Variations within the Glycan Shield of SARS-CoV-2 Impact Viral Spike Dynamics.SARS-CoV-2 糖蛋白聚糖盾的变异影响病毒刺突动力学。
J Mol Biol. 2023 Feb 28;435(4):167928. doi: 10.1016/j.jmb.2022.167928. Epub 2022 Dec 21.
3
Exploring the Potential of Chemical Inhibitors for Targeting Post-translational Glycosylation of Coronavirus (SARS-CoV-2).探索化学抑制剂针对冠状病毒(SARS-CoV-2)翻译后糖基化修饰的潜力。
ACS Omega. 2022 Jul 28;7(31):27038-27051. doi: 10.1021/acsomega.2c02345. eCollection 2022 Aug 9.
4
Spike-heparan sulfate interactions in SARS-CoV-2 infection.刺突糖胺聚糖相互作用在 SARS-CoV-2 感染中的作用。
Curr Opin Struct Biol. 2022 Oct;76:102439. doi: 10.1016/j.sbi.2022.102439. Epub 2022 Jul 6.
5
Engineering ACE2 decoy receptors to combat viral escapability.工程 ACE2 诱饵受体以对抗病毒逃逸。
Trends Pharmacol Sci. 2022 Oct;43(10):838-851. doi: 10.1016/j.tips.2022.06.011. Epub 2022 Jul 25.
6
The Glycan-Binding Trait of the Sarbecovirus Spike N-Terminal Domain Reveals an Evolutionary Footprint.沙贝科病毒刺突 N 端结构域的聚糖结合特性揭示了其进化足迹。
J Virol. 2022 Aug 10;96(15):e0095822. doi: 10.1128/jvi.00958-22. Epub 2022 Jul 19.
7
Pathogen-sugar interactions revealed by universal saturation transfer analysis.普遍饱和转移分析揭示的病原体-糖相互作用。
Science. 2022 Jul 22;377(6604):eabm3125. doi: 10.1126/science.abm3125.
8
Principles of SARS-CoV-2 glycosylation.SARS-CoV-2 糖基化原理。
Curr Opin Struct Biol. 2022 Aug;75:102402. doi: 10.1016/j.sbi.2022.102402. Epub 2022 May 19.
9
Significant role of host sialylated glycans in the infection and spread of severe acute respiratory syndrome coronavirus 2.宿主唾液酸化糖在严重急性呼吸综合征冠状病毒 2 感染和传播中的重要作用。
PLoS Pathog. 2022 Jun 14;18(6):e1010590. doi: 10.1371/journal.ppat.1010590. eCollection 2022 Jun.
10
Synthetic Heparan Sulfate Mimetic Pixatimod (PG545) Potently Inhibits SARS-CoV-2 by Disrupting the Spike-ACE2 Interaction.合成硫酸乙酰肝素模拟物匹克莫德(PG545)通过破坏刺突蛋白与血管紧张素转换酶2的相互作用有效抑制新型冠状病毒。
ACS Cent Sci. 2022 May 25;8(5):527-545. doi: 10.1021/acscentsci.1c01293. Epub 2022 Mar 29.

唾液酸糖缀合物在 SARS-CoV-2 感染中的作用:糖基抑制剂的机遇与挑战。

Involvement of sialoglycans in SARS-COV-2 infection: Opportunities and challenges for glyco-based inhibitors.

机构信息

Department of Biochemistry, Faculty of Science, Mahidol University, Bangkok, Thailand.

Center for Excellence in Protein and Enzyme Technology, Faculty of Science, Mahidol University, Bangkok, Thailand.

出版信息

IUBMB Life. 2022 Dec;74(12):1253-1263. doi: 10.1002/iub.2692. Epub 2022 Nov 19.

DOI:10.1002/iub.2692
PMID:36349722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9877878/
Abstract

Viral infections have been the causes of global pandemics, including the ongoing coronavirus disease 2019, which prompted the investigation into the infection mechanisms to find treatment and aid the vaccine design. Betacoronaviruses use spike glycoprotein on their surface to bind to host receptors, aiding their host attachment and cell fusion. Protein-glycan interaction has been implicated in the viral entry mechanism of many viruses and has recently been shown in SARS-CoV-2. Here, we reviewed the current knowledge on protein-glycan interactions that facilitate SARS-CoV-2 host entry, with special interest in sialoglycans present on both the virions and host cell surfaces. We also analyze how such information provides opportunities and challenges in glyco-based inhibitors.

摘要

病毒感染一直是引发全球大流行的原因,包括正在流行的 2019 年冠状病毒病,这促使人们研究感染机制,以寻找治疗方法并帮助设计疫苗。β冠状病毒利用其表面的刺突糖蛋白与宿主受体结合,帮助其宿主附着和细胞融合。蛋白质-聚糖相互作用已被牵涉到许多病毒的病毒进入机制中,最近在 SARS-CoV-2 中也有显示。在这里,我们综述了促进 SARS-CoV-2 宿主进入的蛋白质-聚糖相互作用的现有知识,特别关注病毒粒子和宿主细胞表面上存在的唾液酸聚糖。我们还分析了这些信息如何在糖基抑制剂方面提供机会和挑战。