亚单位疫苗抗原病毒体展示的模块化方案。

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS STAR Protocols Pub Date : 2025-03-21 Epub Date: 2025-01-31 DOI:10.1016/j.xpro.2025.103610
Victoria C Rosado, Lindsey Adams, Ashraf S Yousif, Maya Sangesland, Larance Ronsard, Vintus Okonkwo, Caitlin McCarthy, Caroline Alexander, Darrell Irvine, Daniel Lingwood
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引用次数: 0

摘要

抗原阵列增加B细胞受体(BCR)触发和亚单位疫苗引起的抗体滴度。在这里,我们提出了一种通过合成病毒体展示多价抗原的方案:预先形成的脂质体携带来自包膜病毒的糖蛋白刺突蛋白。我们描述了如何在预先形成的脂质体中定制脂质化学计量,并通过共价和/或非共价相互作用附加用户定义的抗原。除了产生疫苗研究工具外,该方案还演示了二维膜阵列如何分解和激活异常微弱但关键的病毒受体相互作用。
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A modular protocol for virosome display of subunit vaccine antigens.

Antigen array increases B cell receptor (BCR) triggering and the titer of antibodies elicited by subunit vaccines. Here, we present a protocol for multivalent antigen display by synthetic virosomes: preformed liposomes bearing glycoprotein spike proteins from enveloped viruses. We describe how to customize lipid stoichiometry within preformed liposomes and attach user-defined antigens via covalent and/or non-covalent interactions. In addition to generating vaccine research tools, this protocol demonstrates how two-dimensional membrane array resolves and activates exceptionally weak but critical virus-receptor interactions.

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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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