Severe Acute Respiratory Syndrome Coronavirus 2 Epitope Mapping for Antibodies

Q3 Medicine ImmunoHorizons Pub Date : 2022-06-01 DOI:10.4049/immunohorizons.2200030
Jiaan Yang, Peng Zhang, Wenxiang Cheng, Gang Wu, Q. Niu, Lan Yang, Shun Luo, Xianghua Lin, Lianshan Zhang
{"title":"Severe Acute Respiratory Syndrome Coronavirus 2 Epitope Mapping for Antibodies","authors":"Jiaan Yang, Peng Zhang, Wenxiang Cheng, Gang Wu, Q. Niu, Lan Yang, Shun Luo, Xianghua Lin, Lianshan Zhang","doi":"10.4049/immunohorizons.2200030","DOIUrl":null,"url":null,"abstract":"Epitope mapping of the interactions between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and Abs is challenging because of complexity in protein three-dimensional structures. Protein structure fingerprint technology was applied for epitope mapping of 44 SARS-CoV-2 Abs with three-dimensional structure complexes. The results defined how the epitopes were distributed on SARS-CoV-2 and how the patterns of six CDRs from Abs participated in neutralization. Also, the residue–residue recognition revealed that certain residues had higher frequencies on the interfaces between SARS-CoV-2 and Abs, and the activity correlated with the physicochemical properties of the residues at the interface. Thus, epitope mapping provides significant lead information for development of epitope-based designs for Abs, vaccines, and diagnostic reagents. This is a bioinformatics project of structural data analysis; no animals or cells were used.","PeriodicalId":94037,"journal":{"name":"ImmunoHorizons","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ImmunoHorizons","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.4049/immunohorizons.2200030","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 1

Abstract

Epitope mapping of the interactions between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and Abs is challenging because of complexity in protein three-dimensional structures. Protein structure fingerprint technology was applied for epitope mapping of 44 SARS-CoV-2 Abs with three-dimensional structure complexes. The results defined how the epitopes were distributed on SARS-CoV-2 and how the patterns of six CDRs from Abs participated in neutralization. Also, the residue–residue recognition revealed that certain residues had higher frequencies on the interfaces between SARS-CoV-2 and Abs, and the activity correlated with the physicochemical properties of the residues at the interface. Thus, epitope mapping provides significant lead information for development of epitope-based designs for Abs, vaccines, and diagnostic reagents. This is a bioinformatics project of structural data analysis; no animals or cells were used.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
严重急性呼吸系统综合征冠状病毒2型抗体表位定位
由于蛋白质三维结构的复杂性,严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)与抗体相互作用的表位定位具有挑战性。应用蛋白结构指纹图谱技术对44株具有三维结构复合物的SARS-CoV-2抗体进行表位定位。结果确定了表位在SARS-CoV-2上的分布,以及来自抗体的6种cdr的模式如何参与中和。此外,残基-残基识别结果显示,某些残基在SARS-CoV-2与抗体的界面上具有较高的频率,其活性与界面上残基的物理化学性质相关。因此,表位定位为开发基于表位的抗体、疫苗和诊断试剂设计提供了重要的线索信息。这是一个结构数据分析的生物信息学项目;没有使用动物或细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
3.70
自引率
0.00%
发文量
0
审稿时长
4 weeks
期刊最新文献
Comparison of B Cell Variable Region Gene Segment Characteristics in Neuro-autoantibodies. α-Hemolysin from Staphylococcus aureus Changes the Epigenetic Landscape of Th17 Cells. Estimates of Sequences with Ultralong and Short CDR3s in the Bovine IgM B Cell Receptor Repertoire Using the Long-read Oxford Nanopore MinION Platform. Improving Reliability of Immunological Assays by Defining Minimal Criteria for Cell Fitness. Bruton Tyrosine Kinase Inhibition Decreases Inflammation and Differentially Impacts Phagocytosis and Cellular Metabolism in Mouse- and Human-derived Myeloid Cells.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1