• 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

蛋白质工程应对 COVID-19 大流行。

Protein engineering responses to the COVID-19 pandemic.

机构信息

Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA 78712.

Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA 78712.

出版信息

Curr Opin Struct Biol. 2022 Jun;74:102385. doi: 10.1016/j.sbi.2022.102385. Epub 2022 Apr 11.

DOI:10.1016/j.sbi.2022.102385
PMID:35533563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9075828/
Abstract

Antigen design guided by high-resolution viral glycoprotein structures has successfully generated diverse vaccine candidates for COVID-19. Using conjugation systems to combine antigen design with computationally optimized nanoparticles, researchers have been able to display multivalent antigens with beneficial substitutions that elicited robust humoral immunity with enhanced neutralization potency and breadth. Here, we discuss strategies that have been used for structure-based design and nanoparticle display to develop COVID-19 vaccine candidates as well as potential next-generation vaccine candidates to protect against SARS-CoV-2 variants and other coronaviruses that emerge into the human population.

摘要

基于高分辨率病毒糖蛋白结构的抗原设计成功地为 COVID-19 生成了多种疫苗候选物。研究人员使用缀合系统将抗原设计与经过计算优化的纳米颗粒结合,从而能够展示具有有益取代的多价抗原,这些抗原引发了强大的体液免疫,增强了中和效力和广度。在这里,我们讨论了用于基于结构的设计和纳米颗粒展示的策略,以开发 COVID-19 疫苗候选物以及潜在的下一代疫苗候选物,以预防 SARS-CoV-2 变体和其他进入人类群体的冠状病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5943/9075828/867b502f83a2/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5943/9075828/867b502f83a2/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5943/9075828/867b502f83a2/gr1_lrg.jpg

相似文献

1
Protein engineering responses to the COVID-19 pandemic.蛋白质工程应对 COVID-19 大流行。
Curr Opin Struct Biol. 2022 Jun;74:102385. doi: 10.1016/j.sbi.2022.102385. Epub 2022 Apr 11.
2
RBD decorated PLA nanoparticle admixture with aluminum hydroxide elicit robust and long lasting immune response against SARS-CoV-2.RBD 修饰的 PLA 纳米颗粒混合物与氢氧化铝一起,引发针对 SARS-CoV-2 的强烈和持久的免疫反应。
Eur J Pharm Biopharm. 2022 Jul;176:43-53. doi: 10.1016/j.ejpb.2022.05.008. Epub 2022 May 17.
3
High-Resolution Linear Epitope Mapping of the Receptor Binding Domain of SARS-CoV-2 Spike Protein in COVID-19 mRNA Vaccine Recipients.新型冠状病毒刺突蛋白受体结合域线性表位在 COVID-19 mRNA 疫苗接种者中的高分辨率线性表位作图。
Microbiol Spectr. 2021 Dec 22;9(3):e0096521. doi: 10.1128/Spectrum.00965-21. Epub 2021 Nov 10.
4
Current scenario of COVID-19 vaccinations and immune response along with antibody titer in vaccinated inhabitants of different countries.不同国家接种者的 COVID-19 疫苗接种现状和免疫反应及抗体滴度。
Int Immunopharmacol. 2021 Oct;99:108050. doi: 10.1016/j.intimp.2021.108050. Epub 2021 Aug 6.
5
Insights into COVID-19 Vaccine Development Based on Immunogenic Structural Proteins of SARS-CoV-2, Host Immune Responses, and Herd Immunity.基于 SARS-CoV-2 的免疫原性结构蛋白、宿主免疫反应和群体免疫的 COVID-19 疫苗开发的新见解。
Cells. 2021 Oct 29;10(11):2949. doi: 10.3390/cells10112949.
6
Multivalent Vaccine Strategies in Battling the Emergence of COVID-19 Variants.多价疫苗策略在应对 COVID-19 变异株的出现方面的应用。
Methods Mol Biol. 2022;2511:21-36. doi: 10.1007/978-1-0716-2395-4_2.
7
Hybrid Immunity Shifts the Fc-Effector Quality of SARS-CoV-2 mRNA Vaccine-Induced Immunity.杂合免疫改变了 SARS-CoV-2 mRNA 疫苗诱导免疫的 Fc 效应子质量。
mBio. 2022 Oct 26;13(5):e0164722. doi: 10.1128/mbio.01647-22. Epub 2022 Aug 24.
8
Serum Neutralizing Activity of mRNA-1273 against SARS-CoV-2 Variants.mRNA-1273 对 SARS-CoV-2 变异株的血清中和活性。
J Virol. 2021 Nov 9;95(23):e0131321. doi: 10.1128/JVI.01313-21. Epub 2021 Sep 22.
9
A Single Immunization with Nucleoside-Modified mRNA Vaccines Elicits Strong Cellular and Humoral Immune Responses against SARS-CoV-2 in Mice.单次接种核苷修饰的 mRNA 疫苗可在小鼠中诱导针对 SARS-CoV-2 的强烈细胞和体液免疫应答。
Immunity. 2020 Oct 13;53(4):724-732.e7. doi: 10.1016/j.immuni.2020.07.019. Epub 2020 Jul 30.
10
Current advances and challenges in COVID-19 vaccine development: from conventional vaccines to next-generation vaccine platforms.当前 COVID-19 疫苗研发的进展和挑战:从传统疫苗到下一代疫苗平台。
Mol Biol Rep. 2022 Jun;49(6):4943-4957. doi: 10.1007/s11033-022-07132-7. Epub 2022 Mar 2.

引用本文的文献

1
Mechanistic insights into the structure-based design of a CspZ-targeting Lyme disease vaccine.基于结构设计靶向CspZ的莱姆病疫苗的机制性见解。
Nat Commun. 2025 Apr 7;16(1):2898. doi: 10.1038/s41467-025-58182-x.
2
Mechanistic insights into structure-based design of a Lyme disease subunit vaccine.莱姆病亚单位疫苗基于结构设计的机制性见解
bioRxiv. 2024 Oct 28:2024.10.23.619738. doi: 10.1101/2024.10.23.619738.
3
Engineering a cleaved, prefusion-stabilized influenza B virus hemagglutinin by identification and locking of all six pH switches.

本文引用的文献

1
A human antibody reveals a conserved site on beta-coronavirus spike proteins and confers protection against SARS-CoV-2 infection.一种人类抗体揭示了β冠状病毒刺突蛋白上的一个保守位点,并赋予对SARS-CoV-2感染的保护作用。
Sci Transl Med. 2022 Mar 23;14(637):eabi9215. doi: 10.1126/scitranslmed.abi9215.
2
Stabilized coronavirus spike stem elicits a broadly protective antibody.稳定的冠状病毒刺突茎部引发广泛保护性抗体。
Cell Rep. 2021 Nov 2;37(5):109929. doi: 10.1016/j.celrep.2021.109929. Epub 2021 Oct 16.
3
A novel linear and broadly neutralizing peptide in the SARS-CoV-2 S2 protein for universal vaccine development.
通过识别和锁定所有六个pH开关构建一种裂解的、预融合稳定的乙型流感病毒血凝素
PNAS Nexus. 2024 Oct 11;3(10):pgae462. doi: 10.1093/pnasnexus/pgae462. eCollection 2024 Oct.
4
Multistage protective anti-CelTOS monoclonal antibodies with cross-species sterile protection against malaria.多阶段保护型抗 CelTOS 单克隆抗体,对疟疾具有跨物种的无菌保护作用。
Nat Commun. 2024 Aug 29;15(1):7487. doi: 10.1038/s41467-024-51701-2.
5
Simulation-driven design of stabilized SARS-CoV-2 spike S2 immunogens.基于模拟的稳定 SARS-CoV-2 刺突 S2 免疫原的设计。
Nat Commun. 2024 Aug 27;15(1):7370. doi: 10.1038/s41467-024-50976-9.
6
Development of multidose thermotolerant formulations of a vector-based Covid-19 vaccine candidate, NDV-HXP-S in different product formats: Stability and preservative efficacy study.基于载体的新冠疫苗候选物NDV-HXP-S不同产品形式的多剂量耐热制剂的开发:稳定性和防腐剂功效研究。
Vaccine X. 2024 Jul 27;20:100535. doi: 10.1016/j.jvacx.2024.100535. eCollection 2024 Oct.
7
Opportunities and challenges in design and optimization of protein function.蛋白质功能设计与优化的机遇与挑战。
Nat Rev Mol Cell Biol. 2024 Aug;25(8):639-653. doi: 10.1038/s41580-024-00718-y. Epub 2024 Apr 2.
8
Prefusion-stabilized SARS-CoV-2 S2-only antigen provides protection against SARS-CoV-2 challenge.Prefusion-stabilized SARS-CoV-2 S2-only antigen provides protection against SARS-CoV-2 challenge.
Nat Commun. 2024 Feb 20;15(1):1553. doi: 10.1038/s41467-024-45404-x.
9
Intranasal SARS-CoV-2 RBD decorated nanoparticle vaccine enhances viral clearance in the Syrian hamster model.鼻腔内 SARS-CoV-2 RBD 修饰纳米颗粒疫苗增强了叙利亚仓鼠模型中的病毒清除。
Microbiol Spectr. 2024 Mar 5;12(3):e0499822. doi: 10.1128/spectrum.04998-22. Epub 2024 Feb 9.
10
Surface-modified measles vaccines encoding oligomeric, prefusion-stabilized SARS-CoV-2 spike glycoproteins boost neutralizing antibody responses to Omicron and historical variants, independent of measles seropositivity.表面修饰的麻疹疫苗编码三聚体、预融合稳定的 SARS-CoV-2 刺突糖蛋白,可增强对奥密克戎和历史变异株的中和抗体应答,与麻疹血清阳性无关。
mBio. 2024 Feb 14;15(2):e0292823. doi: 10.1128/mbio.02928-23. Epub 2024 Jan 9.
一种用于通用疫苗开发的新型线性且具有广泛中和作用的肽,存在于新冠病毒S2蛋白中。
Cell Mol Immunol. 2021 Nov;18(11):2563-2565. doi: 10.1038/s41423-021-00778-6. Epub 2021 Oct 13.
4
RBD-homodimer, a COVID-19 subunit vaccine candidate, elicits immunogenicity and protection in rodents and nonhuman primates.RBD-同二聚体,一种新冠病毒亚单位疫苗候选物,在啮齿动物和非人类灵长类动物中引发免疫原性并提供保护。
Cell Discov. 2021 Sep 7;7(1):82. doi: 10.1038/s41421-021-00320-y.
5
Engineered SARS-CoV-2 receptor binding domain improves manufacturability in yeast and immunogenicity in mice.工程化的严重急性呼吸综合征冠状病毒2受体结合域提高了在酵母中的可制造性和在小鼠中的免疫原性。
Proc Natl Acad Sci U S A. 2021 Sep 21;118(38). doi: 10.1073/pnas.2106845118.
6
SARS-CoV-2 variant prediction and antiviral drug design are enabled by RBD in vitro evolution.SARS-CoV-2 变体预测和抗病毒药物设计可通过 RBD 体外进化实现。
Nat Microbiol. 2021 Sep;6(9):1188-1198. doi: 10.1038/s41564-021-00954-4. Epub 2021 Aug 16.
7
Broad betacoronavirus neutralization by a stem helix-specific human antibody.广谱β冠状病毒通过茎螺旋特异性人抗体中和。
Science. 2021 Sep 3;373(6559):1109-1116. doi: 10.1126/science.abj3321. Epub 2021 Aug 6.
8
A non-RBM targeted RBD specific antibody neutralizes SARS-CoV-2 inducing S1 shedding.一种非 RBM 靶向 RBD 特异性抗体中和 SARS-CoV-2 诱导 S1 脱落。
Biochem Biophys Res Commun. 2021 Sep 24;571:152-158. doi: 10.1016/j.bbrc.2021.07.062. Epub 2021 Jul 20.
9
Stabilization of the SARS-CoV-2 Spike Receptor-Binding Domain Using Deep Mutational Scanning and Structure-Based Design.利用深度突变扫描和基于结构的设计稳定 SARS-CoV-2 刺突受体结合结构域。
Front Immunol. 2021 Jun 29;12:710263. doi: 10.3389/fimmu.2021.710263. eCollection 2021.
10
Chimeric spike mRNA vaccines protect against Sarbecovirus challenge in mice.嵌合刺突 mRNA 疫苗可预防小鼠感染 SARS-CoV 属病毒。
Science. 2021 Aug 27;373(6558):991-998. doi: 10.1126/science.abi4506. Epub 2021 Jun 22.