用于即插即用应用的工程化蛋白质-G 变体

bioRxiv Pub Date : 2024-08-08 DOI:10.1101/2024.08.06.606809
Tomasz Slezak, Kelly M. O’Leary, Jinyang Li, A. Rohaim, Elena K. Davydova, A. Kossiakoff
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摘要

我们已开发出一系列基于抗体的模块,这些模块可作为独立单元预制,并以即插即用的方式拼接在一起,形成功能独特强大的多功能组件。这些基本构件来自多对原生和修饰的 Fab 支架和蛋白 G (PG) 变体,这些变体通过噬菌体展示工程引入了高配对特异性。各种可能的 Fab-PG 配对提供了一个高度正交的系统,可用于以简单的方式执行具有挑战性的细胞生物学操作。最简单的表现形式是使用融合了荧光标记 SNAP 标签的 PG 变体进行多重抗原检测。此外,Fabs 可以很容易地连接到 PG-Fc 二聚体模块上,而 PG-Fc 二聚体模块是生产即插即用类 IgG 组合物的核心单元,其用途还可以进一步扩展,利用 "钮入孔 "策略生产双特异性类似物。这些核心 PG-Fc 二聚体模块可以批量生产和储存,只需添加具有所需抗原特异性的 Fab,就能在几分钟内而不是几天或几周内生产出现成的定制 IgG 实体。在另一项应用中,双特异性模式构成了制造强效双特异性 T 细胞激活剂(BiTE)的基石,在癌细胞杀伤试验中证明了它们的功效。此外,该系统还可以将商业抗体作为构建模块,从而大大增加了靶标空间。晶体结构分析表明,Fab-PG 变体对之间的特异性是由几个策略性定位的相互作用产生的,只需做极少的改动就能匹配不同可能组合的支架。这种即插即用的平台为增强细胞生物学研究中基于抗体的试剂的功能提供了一种用户友好型多功能方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Engineered Protein-G variants for plug-and-play applications
We have developed a portfolio of antibody-based modules that can be prefabricated as standalone units and snapped together in plug-and-play fashion to create uniquely powerful multifunctional assemblies. The basic building blocks are derived from multiple pairs of native and modified Fab scaffolds and protein G (PG) variants engineered by phage display to introduce high pair-wise specificity. The variety of possible Fab-PG pairings provides a highly orthogonal system that can be exploited to perform challenging cell biology operations in a straightforward manner. The simplest manifestation allows multiplexed antigen detection using PG variants fused to fluorescently labeled SNAP-tags. Moreover, Fabs can be readily attached to a PG-Fc dimer module which acts as the core unit to produce plug-and-play IgG-like assemblies, and the utility can be further expanded to produce bispecific analogs using the “knobs into holes” strategy. These core PG-Fc dimer modules can be made and stored in bulk to produce off-the-shelf customized IgG entities in minutes, not days or weeks by just adding a Fab with the desired antigen specificity. In another application, the bispecific modalities form the building block for fabricating potent Bispecific T-cell Engagers (BiTEs), demonstrating their efficacy in cancer cell-killing assays. Additionally, the system can be adapted to include commercial antibodies as building blocks, greatly increasing the target space. Crystal structure analysis reveals that a few strategically positioned interactions engender the specificity between the Fab-PG variant pairs, requiring minimal changes to match the scaffolds for different possible combinations. This plug-and-play platform offers a user-friendly and versatile approach to enhance the functionality of antibody-based reagents in cell biology research.
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