• 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

通过中断严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白与血管紧张素转换酶2(ACE2)之间的相互作用来实现SARS-CoV-2早期进入的潜在治疗方法。

Potential therapeutic approaches for the early entry of SARS-CoV-2 by interrupting the interaction between the spike protein on SARS-CoV-2 and angiotensin-converting enzyme 2 (ACE2).

作者信息

Xiang Yusen, Wang Mengge, Chen Hongzhuan, Chen Lili

机构信息

Institute of Interdisciplinary Integrative Medicine Research, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

Institute of Interdisciplinary Integrative Medicine Research, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

出版信息

Biochem Pharmacol. 2021 Oct;192:114724. doi: 10.1016/j.bcp.2021.114724. Epub 2021 Aug 8.

DOI:10.1016/j.bcp.2021.114724
PMID:34371003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8349388/
Abstract

The COVID-19 pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has quickly spread around the globe. At present, there is no precise and effective treatment for the patients with COVID-19, so rapid development of drugs is urgently needed in order to contain the highly infectious disease. The virus spike protein (S protein) can recognize the angiotensin-converting enzyme 2 (ACE2) receptor on the host cell membrane and undergo a series of conformational changes, protease cleavage and membrane fusion to complete the virus entry, so S protein is an important target for vaccine and drug development. Here we provide a brief overview of molecular mechanisms of virus entry, as well as some potential antiviral agents that act on S/ACE2 protein-protein interaction. Specifically, we focused on experimentally validated and/or computational prediction identified inhibitors that target SARS-CoV-2 S protein, ACE2 and enzymes associated with viral infection. This review offers valuable information for the discovery and development of potential antiviral agents in combating SARS-CoV-2. In addition, with the deepening understanding of the mechanism of SARS-CoV-2 infection, more targeted prevention and treatment drugs will be explored with the aid of the advanced technology in the future.

摘要

由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的新型冠状病毒肺炎疫情已在全球迅速蔓延。目前,对于新型冠状病毒肺炎患者尚无精确有效的治疗方法,因此迫切需要快速研发药物以控制这种高传染性疾病。病毒刺突蛋白(S蛋白)可识别宿主细胞膜上的血管紧张素转换酶2(ACE2)受体,并经历一系列构象变化、蛋白酶切割和膜融合以完成病毒进入过程,所以S蛋白是疫苗和药物研发的重要靶点。在此,我们简要概述病毒进入的分子机制,以及一些作用于S/ACE2蛋白-蛋白相互作用的潜在抗病毒药物。具体而言,我们重点关注经实验验证和/或通过计算预测确定的靶向严重急性呼吸综合征冠状病毒2 S蛋白、ACE2以及与病毒感染相关酶的抑制剂。本综述为发现和开发对抗严重急性呼吸综合征冠状病毒2的潜在抗病毒药物提供了有价值的信息。此外,随着对严重急性呼吸综合征冠状病毒2感染机制的深入了解,未来借助先进技术将探索出更多靶向性的预防和治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1437/8349388/4dc04b45c31e/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1437/8349388/9254a202d1b4/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1437/8349388/5bff2ed2b0f1/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1437/8349388/9e69151ce98d/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1437/8349388/fd4f6c81074c/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1437/8349388/4dc04b45c31e/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1437/8349388/9254a202d1b4/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1437/8349388/5bff2ed2b0f1/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1437/8349388/9e69151ce98d/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1437/8349388/fd4f6c81074c/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1437/8349388/4dc04b45c31e/gr4_lrg.jpg

相似文献

1
Potential therapeutic approaches for the early entry of SARS-CoV-2 by interrupting the interaction between the spike protein on SARS-CoV-2 and angiotensin-converting enzyme 2 (ACE2).通过中断严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白与血管紧张素转换酶2(ACE2)之间的相互作用来实现SARS-CoV-2早期进入的潜在治疗方法。
Biochem Pharmacol. 2021 Oct;192:114724. doi: 10.1016/j.bcp.2021.114724. Epub 2021 Aug 8.
2
The Repurposed ACE2 Inhibitors: SARS-CoV-2 Entry Blockers of Covid-19.《再利用 ACE2 抑制剂:COVID-19 的 SARS-CoV-2 进入抑制剂》。
Top Curr Chem (Cham). 2021 Oct 8;379(6):40. doi: 10.1007/s41061-021-00353-7.
3
, and Models for Monitoring SARS-CoV-2 Spike/Human ACE2 Complex, Viral Entry and Cell Fusion.用于监测 SARS-CoV-2 刺突/人 ACE2 复合物、病毒进入和细胞融合的模型。
Viruses. 2021 Feb 25;13(3):365. doi: 10.3390/v13030365.
4
Different compounds against Angiotensin-Converting Enzyme 2 (ACE2) receptor potentially containing the infectivity of SARS-CoV-2: an in silico study.针对血管紧张素转化酶 2(ACE2)受体的不同化合物可能含有 SARS-CoV-2 的感染力:一项计算机研究。
J Mol Model. 2022 Mar 5;28(4):82. doi: 10.1007/s00894-022-05059-1.
5
Possible inhibition of GM-CSF production by SARS-CoV-2 spike-based vaccines.基于新冠病毒刺突蛋白的疫苗可能对粒细胞-巨噬细胞集落刺激因子(GM-CSF)的产生具有抑制作用。
Mol Med. 2021 May 22;27(1):49. doi: 10.1186/s10020-021-00313-3.
6
Repositioning of histamine H receptor antagonist: Doxepin inhibits viropexis of SARS-CoV-2 Spike pseudovirus by blocking ACE2.组胺 H 受体拮抗剂的再定位:多塞平通过阻断 ACE2 抑制 SARS-CoV-2 刺突假病毒的包膜融合。
Eur J Pharmacol. 2021 Apr 5;896:173897. doi: 10.1016/j.ejphar.2021.173897. Epub 2021 Jan 23.
7
In silico investigation of critical binding pattern in SARS-CoV-2 spike protein with angiotensin-converting enzyme 2.计算机模拟研究 SARS-CoV-2 刺突蛋白与血管紧张素转化酶 2 的关键结合模式。
Sci Rep. 2021 Mar 25;11(1):6927. doi: 10.1038/s41598-021-86380-2.
8
Inhibition of S-protein RBD and hACE2 Interaction for Control of SARSCoV- 2 Infection (COVID-19).抑制 S 蛋白 RBD 和 hACE2 相互作用以控制 SARS-CoV-2 感染(COVID-19)。
Mini Rev Med Chem. 2021;21(6):689-703. doi: 10.2174/1389557520666201117111259.
9
An Updated Review on Betacoronavirus Viral Entry Inhibitors: Learning from Past Discoveries to Advance COVID-19 Drug Discovery.贝塔冠状病毒病毒进入抑制剂的最新综述:从过去的发现中吸取教训,推进 COVID-19 药物发现。
Curr Top Med Chem. 2021;21(7):571-596. doi: 10.2174/1568026621666210119111409.
10
Molecular screening of glycyrrhizin-based inhibitors against ACE2 host receptor of SARS-CoV-2.基于甘草酸的抑制剂对新型冠状病毒2型(SARS-CoV-2)ACE2宿主受体的分子筛选
J Mol Model. 2021 Jun 24;27(7):206. doi: 10.1007/s00894-021-04816-y.

引用本文的文献

1
Exploring anti-SARS-CoV-2 natural products: dual-viral target inhibition by delphinidin and the anti-coronaviral efficacy of deapio platycodin D.探索抗SARS-CoV-2天然产物:飞燕草素的双病毒靶点抑制作用及去甲桔梗皂苷D的抗冠状病毒功效
Nat Prod Bioprospect. 2025 Jun 13;15(1):39. doi: 10.1007/s13659-025-00523-w.
2
Development of SARS-CoV-2 entry antivirals.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)进入抑制剂的研发。
Cell Insight. 2024 Jan 30;3(1):100144. doi: 10.1016/j.cellin.2023.100144. eCollection 2024 Feb.
3
Relationship between Vitamin D and Immunity in Older People with COVID-19.

本文引用的文献

1
Berbamine inhibits SARS-CoV-2 infection by compromising TRPMLs-mediated endolysosomal trafficking of ACE2.小檗胺通过破坏瞬时受体电位阳离子通道M型(TRPMLs)介导的血管紧张素转换酶2(ACE2)的内溶酶体运输来抑制新型冠状病毒2(SARS-CoV-2)感染。
Signal Transduct Target Ther. 2021 Apr 24;6(1):168. doi: 10.1038/s41392-021-00584-6.
2
SARS-CoV-2 spike E484K mutation reduces antibody neutralisation.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白E484K突变降低抗体中和作用。
Lancet Microbe. 2021 Jul;2(7):e283-e284. doi: 10.1016/S2666-5247(21)00068-9. Epub 2021 Apr 7.
3
Drug Repurposing of Itraconazole and Estradiol Benzoate against COVID-19 by Blocking SARS-CoV-2 Spike Protein-Mediated Membrane Fusion.
维生素 D 与 COVID-19 老年患者免疫功能的关系。
Int J Environ Res Public Health. 2023 Apr 7;20(8):5432. doi: 10.3390/ijerph20085432.
4
Targeting SARS-CoV-2 and host cell receptor interactions.靶向 SARS-CoV-2 与宿主细胞受体相互作用。
Antiviral Res. 2023 Feb;210:105514. doi: 10.1016/j.antiviral.2022.105514. Epub 2022 Dec 26.
5
Ginkgolic acids inhibit SARS-CoV-2 and its variants by blocking the spike protein/ACE2 interplay.银杏酸通过阻断刺突蛋白/ACE2 相互作用来抑制 SARS-CoV-2 及其变体。
Int J Biol Macromol. 2023 Jan 31;226:780-792. doi: 10.1016/j.ijbiomac.2022.12.057. Epub 2022 Dec 12.
6
Small molecules in the treatment of COVID-19.小分子药物治疗 COVID-19。
Signal Transduct Target Ther. 2022 Dec 5;7(1):387. doi: 10.1038/s41392-022-01249-8.
7
Resistance profile and mechanism of severe acute respiratory syndrome coronavirus-2 variants to LCB1 inhibitor targeting the spike receptor-binding motif.严重急性呼吸综合征冠状病毒2变体对靶向刺突受体结合基序的LCB1抑制剂的抗性概况及机制
Front Microbiol. 2022 Oct 11;13:1022006. doi: 10.3389/fmicb.2022.1022006. eCollection 2022.
8
ADAM and ADAMTS disintegrin and metalloproteinases as major factors and molecular targets in vascular malfunction and disease.ADAM 和 ADAMTS 解整合素金属蛋白酶作为血管功能障碍和疾病的主要因素和分子靶点。
Adv Pharmacol. 2022;94:255-363. doi: 10.1016/bs.apha.2021.11.002. Epub 2022 Jan 24.
通过阻断严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白介导的膜融合,将伊曲康唑和苯甲酸雌二醇用于新型冠状病毒肺炎的药物重新利用
Adv Ther (Weinh). 2021 May;4(5):2000224. doi: 10.1002/adtp.202000224. Epub 2021 Feb 22.
4
Immunity to SARS-CoV-2 variants of concern.对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)关注变异株的免疫力。
Science. 2021 Mar 12;371(6534):1103-1104. doi: 10.1126/science.abg7404.
5
Circulating SARS-CoV-2 spike N439K variants maintain fitness while evading antibody-mediated immunity.循环 Sars-CoV-2 刺突 N439K 变体在保持适应性的同时逃避抗体介导的免疫。
Cell. 2021 Mar 4;184(5):1171-1187.e20. doi: 10.1016/j.cell.2021.01.037. Epub 2021 Jan 28.
6
Screening and evaluation of anti-SARS-CoV-2 components from Ephedra sinica by ACE2/CMC-HPLC-IT-TOF-MS approach.采用 ACE2/CMC-HPLC-IT-TOF-MS 方法从麻黄中筛选和评价抗 SARS-CoV-2 成分。
Anal Bioanal Chem. 2021 May;413(11):2995-3004. doi: 10.1007/s00216-021-03233-7. Epub 2021 Feb 19.
7
Kobophenol A Inhibits Binding of Host ACE2 Receptor with Spike RBD Domain of SARS-CoV-2, a Lead Compound for Blocking COVID-19.Kobophenol A 抑制 SARS-CoV-2 刺突 RBD 结构域与宿主 ACE2 受体结合,是一种用于阻断 COVID-19 的先导化合物。
J Phys Chem Lett. 2021 Feb 25;12(7):1793-1802. doi: 10.1021/acs.jpclett.0c03119. Epub 2021 Feb 12.
8
Safety, tolerability, and immunogenicity of an inactivated SARS-CoV-2 vaccine (CoronaVac) in healthy adults aged 60 years and older: a randomised, double-blind, placebo-controlled, phase 1/2 clinical trial.一种灭活严重急性呼吸综合征冠状病毒2疫苗(科兴新冠疫苗)在60岁及以上健康成年人中的安全性、耐受性和免疫原性:一项随机、双盲、安慰剂对照的1/2期临床试验
Lancet Infect Dis. 2021 Jun;21(6):803-812. doi: 10.1016/S1473-3099(20)30987-7. Epub 2021 Feb 3.
9
Blocking Effect of Demethylzeylasteral on the Interaction between Human ACE2 Protein and SARS-CoV-2 RBD Protein Discovered Using SPR Technology.利用 SPR 技术发现去甲基泽拉木醛对人 ACE2 蛋白与 SARS-CoV-2 RBD 蛋白相互作用的阻断作用。
Molecules. 2020 Dec 24;26(1):57. doi: 10.3390/molecules26010057.
10
Protoporphyrin IX and verteporfin potently inhibit SARS-CoV-2 infection and in a mouse model expressing human ACE2.原卟啉IX和维替泊芬在表达人血管紧张素转换酶2的小鼠模型中能有效抑制严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染。
Sci Bull (Beijing). 2021 May 15;66(9):925-936. doi: 10.1016/j.scib.2020.12.005. Epub 2020 Dec 9.