单生物素化蛋白拴在微球上检测抗原特异性血清抗体。

Journal of biological methods Pub Date : 2022-09-23 eCollection Date: 2021-01-01 DOI:10.14440/jbm.2022.390
Caleb S Whitley, Thomas C Mitchell
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引用次数: 0

摘要

表面修饰的微球已被用作固定抗原的有用方法,用于血清学研究。羧基修饰微球用于这一目的的使用是公认的,但通常与技术挑战有关。链霉亲和素修饰的微球几乎不需要专业技术,因此解决了羧基微球的一些缺点。链霉亲和素微球的另一个特点是使用单生物素化蛋白,该蛋白在C末端含有单个生物素化基序。然而,链亲和素和羧基微球的相对性能尚不清楚。在这里,我们对链霉亲和素和羧基微球进行了头对头的比较。我们比较了抗原结合、定向和染色质量,发现基于这些定义的参数,两种微球的表现相似。我们还评估了与严重急性呼吸综合征冠状病毒2型受体结合结构域(RBD)结合的链霉亲和素微球的实用性,以可靠地检测最近用辉瑞/BioNTech信使核糖核酸冠状病毒病(COVID)疫苗免疫的个体产生的RBD特异性IgG1、IgG3和IgA1,作为“概念证明”。我们提供的证据表明,使用RBD包被的微球、Ig特异性“检测”单克隆抗体(mAb)和流式细胞术,每个抗体靶点在血清中都是可检测的。我们发现,通过抗体滴定可以使检测mAb的交叉反应性最小化,以改善IgG1和IgG3之间的分化。我们还用严重急性呼吸系统综合征冠状病毒2型德尔塔变异RBD包被了链亲和素微球,以确定链亲和素-微球方法是否显示免疫血清抗体与野生型(武汉)和变异RBD(德尔塔)的结合有任何差异。总的来说,我们的结果表明,负载单生物素化抗原的链霉亲和素微球是用于血清学测定的化学交联抗原-羧基微球的有力替代品。
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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Monobiotinylated Proteins Tethered to Microspheres for Detection of Antigen-Specific Serum Antibodies.

Surface modified microspheres have been leveraged as a useful way to immobilize antigen for serological studies. The use of carboxyl modified microspheres for this purpose is well-established, but commonly associated with technical challenges. Streptavidin modified microspheres require little technical expertise and thus address some of the shortcomings of carboxyl microspheres. An additional feature of streptavidin microspheres is the use of mono-biotinylated proteins, which contain a single biotinylation motif at the C-terminus. However, the relative performance of streptavidin and carboxyl microspheres is unknown. Here, we performed a head-to-head comparison of streptavidin and carboxyl microspheres. We compared antigen binding, orientation, and staining quality and found that both microspheres perform similarly based on these defined parameters. We also evaluated the utility of streptavidin microspheres bound to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) receptor binding domain (RBD), to reliably detect RBD-specific IgG1, IgG3, and IgA1 produced in individuals recently immunized with Pfizer/BioNTech mRNA coronavirus disease (COVID) vaccine as 'proof-of-concept'. We provide evidence that each of the antibody targets are detectable in serum using RBD-coated microspheres, Ig-specific 'detector' monoclonal antibodies (mAbs), and flow cytometry. We found that cross-reactivity of the detector mAbs can be minimized by antibody titration to improve differentiation between IgG1 and IgG3. We also coated streptavidin microspheres with SARS-CoV-2 delta variant RBD to determine if the streptavidin microsphere approach revealed any differences in binding of immune serum antibodies to wild-type (Wuhan) versus variant RBD (Delta). Overall, our results show that streptavidin microspheres loaded with mono-biotinylated antigen is a robust alternative to chemically cross-linking antigen to carboxyl microspheres for use in serological assays.

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