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蛋白质表位作图的氢氘交换质谱研究进展。

Research advances in hydrogen-deuterium exchange mass spectrometry for protein epitope mapping.

机构信息

National Institute of Metrology, Beijing, 100029, China.

College of Chemistry, Beijing University of Chemical Technology, Beijing, 100029, China.

出版信息

Anal Bioanal Chem. 2021 Apr;413(9):2345-2359. doi: 10.1007/s00216-020-03091-9. Epub 2021 Jan 6.

DOI:10.1007/s00216-020-03091-9
PMID:33404742
Abstract

With the development of biomedical technology, epitope mapping of proteins has become critical for developing and evaluating new protein drugs. The application of hydrogen-deuterium exchange for protein epitope mapping holds great potential. Although several reviews addressed the hydrogen-deuterium exchange, to date, only a few systematic reviews have focused on epitope mapping using this technology. Here, we introduce the basic principles, development history, and review research progress in hydrogen-deuterium exchange epitope mapping technology and discuss its advantages. We summarize the main hurdles in applying hydrogen-deuterium exchange epitope mapping technology, combined with relevant examples to provide specific solutions. We describe the epitope mapping of virus assemblies, disease-associated proteins, and polyclonal antibodies as examples of pattern introduction. Finally, we discuss the outlook of hydrogen-deuterium exchange epitope mapping technology. This review will help researchers studying protein epitopes to gain a more comprehensive understanding of this technology.

摘要

随着生物医学技术的发展,蛋白质表位作图对于开发和评估新型蛋白质药物至关重要。氢氘交换在蛋白质表位作图中的应用具有巨大的潜力。尽管有几篇综述讨论了氢氘交换,但迄今为止,只有少数系统综述专注于使用该技术进行表位作图。在这里,我们介绍了氢氘交换表位作图技术的基本原理、发展历史和综述研究进展,并讨论了它的优势。我们总结了应用氢氘交换表位作图技术的主要障碍,并结合相关实例提供了具体的解决方案。我们以病毒组装体、疾病相关蛋白和多克隆抗体的表位作图为例进行模式介绍。最后,我们讨论了氢氘交换表位作图技术的展望。本综述将帮助研究蛋白质表位的研究人员更全面地了解这项技术。

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Mapping binding epitopes of monoclonal antibodies targeting major histocompatibility complex class I chain-related A (MICA) with hydrogen/deuterium exchange and electron-transfer dissociation mass spectrometry.应用氢/氘交换和电子转移解离质谱技术绘制针对主要组织相容性复合体Ⅰ类链相关 A(MICA)的单克隆抗体的结合表位图谱。
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使用毫秒级氢/氘交换质谱法重新校准保护因子
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