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基于电镜的多克隆表位作图分析糖蛋白抗原抗体反应的方案。

Protocol for analyzing antibody responses to glycoprotein antigens using electron-microscopy-based polyclonal epitope mapping.

机构信息

Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.

Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.

出版信息

STAR Protoc. 2023 Sep 15;4(3):102476. doi: 10.1016/j.xpro.2023.102476. Epub 2023 Jul 28.

Abstract

Electron microscopy-based polyclonal epitope mapping (EMPEM) can delineate epitope specificities of serum antibodies to a given antigen following vaccination or infection. Here, we present a protocol for the EMPEM method for rapid high-throughput assessment of antibody responses to glycoprotein antigens in vaccination and infection studies. We describe steps for antibody isolation and digestion, antigen complex and purification, and electron microscope imaging. We then detail procedures for processing and analysis of EMPEM data. For complete details on the use and execution of this protocol, please refer to Bianchi et al. (2018)..

摘要

基于电子显微镜的多克隆表位作图(EMPEM)可以描绘接种疫苗或感染后针对特定抗原的血清抗体的表位特异性。在这里,我们提供了一种用于快速高通量评估疫苗接种和感染研究中糖蛋白抗原抗体反应的 EMPEM 方法的方案。我们描述了抗体分离和消化、抗原复合物和纯化以及电子显微镜成像的步骤。然后,我们详细介绍了 EMPEM 数据的处理和分析程序。有关此方案的使用和执行的完整详细信息,请参见 Bianchi 等人。(2018)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d53a/10400963/e9154ec4632e/fx1.jpg

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