Using Open-Source Bioinformatics and Visualization Tools to Explore the Structure and Function of SARS-CoV-2 Spike Protein

CourseSource Pub Date : 2022-01-01 DOI:10.24918/cs.2022.5
L. Listenberger, C. Joiner, C. Terrell
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Abstract

The relationship between protein structure and function is a foundational concept in undergraduate biochemistry. We find this theme is best presented with assignments that encourage exploration and analysis. Here, we share a series of four assignments that use open-source, online molecular visualization and bioinformatics tools to examine the interaction between the SARSCoV-2 spike protein and the ACE2 receptor. The interaction between these two proteins initiates SARS-CoV-2 infection of human host cells and is the cause of COVID-19. In assignment I, students identify sequences with homology to the SARSCoV-2 spike protein and use them to build a primary sequence alignment. Students make connections to a linked primary research article as an example of how scientists use molecular and phylogenetic analysis to explore the origins of a novel virus. Assignments II through IV teach students to use an online molecular visualization tool for analysis of secondary, tertiary, and quaternary structure. Emphasis is placed on identification of noncovalent interactions that stabilize the SARS-CoV-2 spike protein and mediate its interaction with ACE2. We assigned this project to upper-level undergraduate biochemistry students at a public university and liberal arts college. Students in our courses completed the project as individual homework assignments. However, we can easily envision implementation of this project during multiple in-class sessions or in a biochemistry laboratory using in-person or remote learning. We share this project as a resource for instructors who aim to teach protein structure and function using inquiry-based molecular visualization activities. Citation: Listenberger LL, Joiner CM, Terrell CR. 2022. Using open-source bioinformatics and visualization tools to explore the structure and function of SARS-CoV-2 spike protein. CourseSource. https://doi.org/10.24918/cs.2022.5 Editor: Charles Hauser, St. Edward’s University Received: 1/5/2021; Accepted: 9/9/2021; Published: 3/18/2022 Copyright: © 2022 Listenberger, Joiner, and Terrell. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited. The images used in supporting materials (Supporting File S3: Molecular Modeling – Summative Assessments and Data from Student Responses) are from journals that use the Creative Commons Attribution License. We cite the original source for each figure. The primary image includes student generated data and a cartoon from Pixabay, an online repository of copyright free art. Conflict of Interest and Funding Statement: None of the authors has a financial, personal, or professional conflict of interest related to this work. Supporting Materials: Supporting Files S1. Molecular Modeling – BioMolViz Goals and Objectives; S2. Molecular Modeling – Assignments I-IV; S3. Molecular Modeling – Summative Assessments and Data from Student Responses; S4. Molecular Modeling – Answer Key (contact corresponding author for a copy); and S5. Molecular Modeling – Teaching Resources. *Correspondence to: University of Minnesota, Center for Learning Innovation, 111 S. Broadway, Rochester, MN, 55904, terre031@r.umn.edu. CourseSource | www.coursesource.org 2022 | Volume 09 1 Lesson
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利用开源生物信息学和可视化工具探索SARS-CoV-2刺突蛋白的结构和功能
蛋白质结构与功能的关系是本科生物化学的一个基本概念。我们发现这个主题最好是通过鼓励探索和分析的作业来呈现。在这里,我们分享了一系列的四个作业,使用开源,在线分子可视化和生物信息学工具来检查SARSCoV-2刺突蛋白和ACE2受体之间的相互作用。这两种蛋白之间的相互作用启动了人类宿主细胞的SARS-CoV-2感染,是COVID-19的原因。在作业1中,学生识别与SARSCoV-2刺突蛋白同源的序列,并用它们建立初级序列比对。学生将一篇相关的初级研究文章作为科学家如何使用分子和系统发育分析来探索新型病毒起源的例子。作业二至作业四教学生使用在线分子可视化工具分析二级、三级和四级结构。重点是鉴定稳定SARS-CoV-2刺突蛋白并介导其与ACE2相互作用的非共价相互作用。我们将这个项目分配给一所公立大学和文理学院的高年级生物化学本科生。我们课程的学生将这个项目作为个人家庭作业来完成。然而,我们可以很容易地设想在多个课堂上或在生物化学实验室中使用面对面或远程学习来实现这个项目。我们分享这个项目作为教师的资源,他们的目标是使用基于探究式的分子可视化活动来教授蛋白质的结构和功能。引用本文:Listenberger LL, Joiner CM, Terrell CR. 2022。利用开源生物信息学和可视化工具探索SARS-CoV-2刺突蛋白的结构和功能。CourseSource。https://doi.org/10.24918/cs.2022.5编辑:Charles Hauser, St. Edward 's University收稿日期:1/5/2021;接受:9/9/2021;版权所有:©2022 Listenberger, Joiner, and Terrell。这是一篇在知识共享署名-非商业-相同方式共享4.0国际许可协议下发布的开放获取文章,该协议允许在任何媒体上不受限制的非商业使用、分发和复制,前提是要注明原作者和来源。支持材料(支持文件S3:分子建模-总结性评估和学生反馈数据)中使用的图像来自使用知识共享署名许可的期刊。我们引用了每个数字的原始来源。主图像包括学生生成的数据和来自Pixabay的漫画,Pixabay是一个免费的在线艺术存储库。利益冲突和资金声明:作者没有与本研究相关的财务、个人或专业利益冲突。支持材料:支持文件分子建模- BioMolViz目标和目的;S2。分子建模-作业I-IV;S3。分子建模-总结性评估和学生反应数据S4。分子建模-答案键(副本请联系通讯作者);和S5。分子建模-教学资源。*通讯地址:明尼苏达大学学习创新中心,111 S. Broadway, Rochester, MN, 55904, terre031@r.umn.edu。课程来源| www.coursesource.org 2022 |卷09 1课
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