tANCHOR fast and cost-effective cell-based immunization approach with focus on the receptor-binding domain of SARS-CoV-2.

IF 2.5 Q3 BIOCHEMICAL RESEARCH METHODS
Biology Methods and Protocols Pub Date : 2023-12-12 eCollection Date: 2023-01-01 DOI:10.1093/biomethods/bpad030
Hubert Bernauer, Anja Schlör, Josef Maier, Norbert Bannert, Katja Hanack, Daniel Ivanusic
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引用次数: 0

Abstract

Successful induction of antibodies in model organisms like mice depends strongly on antigen design and delivery. New antigen designs for immunization are helpful for developing future therapeutic monoclonal antibodies (mAbs). One of the gold standards to induce antibodies in mice is to express and purify the antigen for vaccination. This is especially time-consuming when mAbs are needed rapidly. We closed this gap and used the display technology tetraspanin anchor to develop a reliable immunization technique without the need to purify the antigen. This technique is able to speed up the immunization step enormously and we have demonstrated that we were able to induce antibodies against different proteins with a focus on the receptor-binding domain of SARS-CoV-2 and the extracellular loop of canine cluster of differentiation 20 displayed on the surface of human cells.

tANCHOR 以 SARS-CoV-2 的受体结合域为重点的快速、经济的细胞免疫方法。
在小鼠等模式生物体内成功诱导抗体在很大程度上取决于抗原的设计和递送。用于免疫的新抗原设计有助于开发未来的治疗性单克隆抗体(mAbs)。诱导小鼠产生抗体的黄金标准之一是表达和纯化用于疫苗接种的抗原。当需要快速获得 mAbs 时,这尤其耗时。我们填补了这一空白,利用四泛素锚显示技术开发出一种无需纯化抗原的可靠免疫技术。这项技术能够大大加快免疫步骤,我们已经证明,我们能够诱导出针对不同蛋白质的抗体,重点是 SARS-CoV-2 的受体结合域和显示在人类细胞表面的犬分化簇 20 的胞外环。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biology Methods and Protocols
Biology Methods and Protocols Agricultural and Biological Sciences-Agricultural and Biological Sciences (all)
CiteScore
3.80
自引率
2.80%
发文量
28
审稿时长
19 weeks
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