• 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

SARS-CoV-2 刺突蛋白突变探索者:使用互动应用程序提高公众对 SARS-CoV-2 关注变异株的理解。

The SARS-CoV-2 Spike Protein Mutation Explorer: using an interactive application to improve the public understanding of SARS-CoV-2 variants of concern.

机构信息

School of Simulation and Visualisation, The Glasgow School of Art, Glasgow, UK.

MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.

出版信息

J Vis Commun Med. 2023 Jul;46(3):122-132. doi: 10.1080/17453054.2023.2237087. Epub 2023 Aug 1.

DOI:10.1080/17453054.2023.2237087
PMID:37526402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10726978/
Abstract

Due to the COVID-19 pandemic the virus responsible, SARS-CoV-2, became a source of intense interest for non-expert audiences. The viral spike protein gained particular public interest as the main target for protective immune responses, including those elicited by vaccines. The rapid evolution of SARS-CoV-2 resulted in variations in the spike that enhanced transmissibility or weakened vaccine protection. This created new variants of concern (VOCs). The emergence of VOCs was studied using viral sequence data which was shared through portals such as the online Mutation Explorer of the COVID-19 Genomics UK consortium (COG-UK/ME). This was designed for an expert audience, but the information it contained could be of general interest if suitably communicated. Visualisations, interactivity and animation can improve engagement and understanding of molecular biology topics, and so we developed a graphical educational resource, the SARS-CoV-2 Spike Protein Mutation Explorer (SSPME), which used interactive 3D molecular models and animations to explain the molecular biology underpinning VOCs. User testing showed that the SSPME had better usability and improved participant knowledge confidence and knowledge acquisition compared to COG-UK/ME. This demonstrates how interactive visualisations can be used for effective molecular biology communication, as well as improving the public understanding of SARS-CoV-2 VOCs.

摘要

由于 COVID-19 大流行,导致其元凶 SARS-CoV-2 成为了非专业人士关注的焦点。病毒的刺突蛋白引起了公众的特别兴趣,因为它是保护性免疫反应的主要目标,包括疫苗引起的反应。SARS-CoV-2 的快速进化导致刺突蛋白发生变异,从而增强了传染性或削弱了疫苗的保护作用。这就产生了新的关注变种(VOCs)。通过在线 COVID-19 基因组英国联盟(COG-UK/ME)的突变探索器等门户共享的病毒序列数据来研究 VOCs 的出现。该数据旨在面向专家受众,但如果以适当的方式进行交流,其中包含的信息也可能具有普遍的兴趣。可视化、交互性和动画可以提高对分子生物学主题的参与度和理解度,因此我们开发了一个图形教育资源,即 SARS-CoV-2 刺突蛋白突变探索器(SSPME),它使用交互式 3D 分子模型和动画来解释 VOCs 背后的分子生物学。用户测试表明,与 COG-UK/ME 相比,SSPME 具有更好的可用性,并且提高了参与者的知识信心和知识获取。这证明了交互式可视化如何用于有效的分子生物学交流,以及提高公众对 SARS-CoV-2 VOCs 的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/42871e22d8dc/IJAU_A_2237087_F0006_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/92e9c193cc55/IJAU_A_2237087_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/70312a026775/IJAU_A_2237087_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/8610fb603abd/IJAU_A_2237087_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/eaf223e242cf/IJAU_A_2237087_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/bcb1058fd761/IJAU_A_2237087_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/42871e22d8dc/IJAU_A_2237087_F0006_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/92e9c193cc55/IJAU_A_2237087_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/70312a026775/IJAU_A_2237087_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/8610fb603abd/IJAU_A_2237087_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/eaf223e242cf/IJAU_A_2237087_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/bcb1058fd761/IJAU_A_2237087_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424f/10726978/42871e22d8dc/IJAU_A_2237087_F0006_C.jpg

相似文献

1
The SARS-CoV-2 Spike Protein Mutation Explorer: using an interactive application to improve the public understanding of SARS-CoV-2 variants of concern.SARS-CoV-2 刺突蛋白突变探索者:使用互动应用程序提高公众对 SARS-CoV-2 关注变异株的理解。
J Vis Commun Med. 2023 Jul;46(3):122-132. doi: 10.1080/17453054.2023.2237087. Epub 2023 Aug 1.
2
Using Molecular Visualisation Techniques to Explain the Molecular Biology of SARS-CoV-2 Spike Protein Mutations to a General Audience.利用分子可视化技术向普通受众解释 SARS-CoV-2 刺突蛋白突变的分子生物学。
Adv Exp Med Biol. 2022;1388:129-152. doi: 10.1007/978-3-031-10889-1_6.
3
Emerging Variants of SARS-CoV-2 and Novel Therapeutics Against Coronavirus (COVID-19)严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的新变种及针对冠状病毒(COVID-19)的新型疗法
4
COVID-19 CG enables SARS-CoV-2 mutation and lineage tracking by locations and dates of interest.COVID-19 CG 通过关注的地点和日期来实现 SARS-CoV-2 的突变和谱系追踪。
Elife. 2021 Feb 23;10:e63409. doi: 10.7554/eLife.63409.
5
Emergency SARS-CoV-2 Variants of Concern: Novel Multiplex Real-Time RT-PCR Assay for Rapid Detection and Surveillance.关注的紧急 SARS-CoV-2 变异株:用于快速检测和监测的新型多重实时 RT-PCR 检测方法。
Microbiol Spectr. 2022 Feb 23;10(1):e0251321. doi: 10.1128/spectrum.02513-21.
6
SARS-CoV2 variant-specific replicating RNA vaccines protect from disease following challenge with heterologous variants of concern.SARS-CoV-2 变异株特异性复制 RNA 疫苗可预防同源关切变异株挑战后的疾病。
Elife. 2022 Feb 22;11:e75537. doi: 10.7554/eLife.75537.
7
Effects of Spike Mutations in SARS-CoV-2 Variants of Concern on Human or Animal ACE2-Mediated Virus Entry and Neutralization.关注的 SARS-CoV-2 变异株刺突突变对人类或动物 ACE2 介导的病毒进入和中和的影响。
Microbiol Spectr. 2022 Jun 29;10(3):e0178921. doi: 10.1128/spectrum.01789-21. Epub 2022 May 31.
8
Real-Time RT-PCR Allelic Discrimination Assay for Detection of N501Y Mutation in the Spike Protein of SARS-CoV-2 Associated with B.1.1.7 Variant of Concern.实时 RT-PCR 等位基因鉴别检测法用于检测与关注变异株 B.1.1.7 相关的 SARS-CoV-2 刺突蛋白 N501Y 突变。
Microbiol Spectr. 2022 Feb 23;10(1):e0068121. doi: 10.1128/spectrum.00681-21. Epub 2022 Feb 16.
9
Cross-Neutralization of Emerging SARS-CoV-2 Variants of Concern by Antibodies Targeting Distinct Epitopes on Spike.靶向刺突蛋白不同表位的抗体对新型 SARS-CoV-2 关切变异株的交叉中和作用
mBio. 2021 Dec 21;12(6):e0297521. doi: 10.1128/mBio.02975-21. Epub 2021 Nov 16.
10
Escape from neutralizing antibodies by SARS-CoV-2 spike protein variants.通过 SARS-CoV-2 刺突蛋白变体逃避中和抗体。
Elife. 2020 Oct 28;9:e61312. doi: 10.7554/eLife.61312.

本文引用的文献

1
Using Molecular Visualisation Techniques to Explain the Molecular Biology of SARS-CoV-2 Spike Protein Mutations to a General Audience.利用分子可视化技术向普通受众解释 SARS-CoV-2 刺突蛋白突变的分子生物学。
Adv Exp Med Biol. 2022;1388:129-152. doi: 10.1007/978-3-031-10889-1_6.
2
SARS-CoV-2 variants, spike mutations and immune escape.SARS-CoV-2 变体、刺突突变和免疫逃逸。
Nat Rev Microbiol. 2021 Jul;19(7):409-424. doi: 10.1038/s41579-021-00573-0. Epub 2021 Jun 1.
3
SARS-CoV-2 one year on: evidence for ongoing viral adaptation.
SARS-CoV-2 一年来的发展:病毒持续适应的证据。
J Gen Virol. 2021 Apr;102(4). doi: 10.1099/jgv.0.001584.
4
Beyond Shielding: The Roles of Glycans in the SARS-CoV-2 Spike Protein.超越屏蔽作用:聚糖在新冠病毒刺突蛋白中的作用
ACS Cent Sci. 2020 Oct 28;6(10):1722-1734. doi: 10.1021/acscentsci.0c01056. Epub 2020 Sep 23.
5
Receptor binding and priming of the spike protein of SARS-CoV-2 for membrane fusion.SARS-CoV-2 刺突蛋白的受体结合和引发膜融合。
Nature. 2020 Dec;588(7837):327-330. doi: 10.1038/s41586-020-2772-0. Epub 2020 Sep 17.
6
Structures and distributions of SARS-CoV-2 spike proteins on intact virions.完整病毒上 SARS-CoV-2 刺突蛋白的结构和分布。
Nature. 2020 Dec;588(7838):498-502. doi: 10.1038/s41586-020-2665-2. Epub 2020 Aug 17.
7
SARS-CoV-2 and bat RaTG13 spike glycoprotein structures inform on virus evolution and furin-cleavage effects.SARS-CoV-2 和蝙蝠 RaTG13 刺突糖蛋白结构阐明了病毒进化和弗林蛋白酶切割的影响。
Nat Struct Mol Biol. 2020 Aug;27(8):763-767. doi: 10.1038/s41594-020-0468-7. Epub 2020 Jul 9.
8
Developing a Fully Glycosylated Full-Length SARS-CoV-2 Spike Protein Model in a Viral Membrane.在病毒膜中构建完全糖基化全长 SARS-CoV-2 刺突蛋白模型。
J Phys Chem B. 2020 Aug 20;124(33):7128-7137. doi: 10.1021/acs.jpcb.0c04553. Epub 2020 Jul 6.
9
Structural basis for the recognition of SARS-CoV-2 by full-length human ACE2.全长人血管紧张素转化酶 2 识别 SARS-CoV-2 的结构基础。
Science. 2020 Mar 27;367(6485):1444-1448. doi: 10.1126/science.abb2762. Epub 2020 Mar 4.
10
Functional assessment of cell entry and receptor usage for SARS-CoV-2 and other lineage B betacoronaviruses.SARS-CoV-2 及其他 B 属β冠状病毒的细胞进入和受体使用功能评估。
Nat Microbiol. 2020 Apr;5(4):562-569. doi: 10.1038/s41564-020-0688-y. Epub 2020 Feb 24.