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Novel Regeneration Approach for Creating Reusable FO-SPR Probes with NTA Surface Chemistry

机译:NTA表面化学创造可重复使用的FO-SCR探针的新型再生方法

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摘要

To date, surface plasmon resonance (SPR) biosensors have been exploited in numerous different contexts while continuously pushing boundaries in terms of improved sensitivity, specificity, portability and reusability. The latter has attracted attention as a viable alternative to disposable biosensors, also offering prospects for rapid screening of biomolecules or biomolecular interactions. In this context here, we developed an approach to successfully regenerate a fiber-optic (FO)-SPR surface when utilizing cobalt (II)-nitrilotriacetic acid (NTA) surface chemistry. To achieve this, we tested multiple regeneration conditions that can disrupt the NTA chelate on a surface fully saturated with His6-tagged antibody fragments (scFv-33H1F7) over ten regeneration cycles. The best surface regeneration was obtained when combining 100 mM EDTA, 500 mM imidazole and 0.5% SDS at pH 8.0 for 1 min with shaking at 150 rpm followed by washing with 0.5 M NaOH for 3 min. The true versatility of the established approach was proven by regenerating the NTA surface for ten cycles with three other model system bioreceptors, different in their size and structure: His6-tagged SARS-CoV-2 spike fragment (receptor binding domain, RBD), a red fluorescent protein (RFP) and protein origami carrying 4 RFPs (Tet12SN-RRRR). Enabling the removal of His6-tagged bioreceptors from NTA surfaces in a fast and cost-effective manner can have broad applications, spanning from the development of biosensors and various biopharmaceutical analyses to the synthesis of novel biomaterials.
机译:迄今为止,表面等离子体共振(SPR)生物传感器已经在许多不同的背景下被利用,同时在提高灵敏度,特异性,可移植性和可重用性方面连续推动边界。后者引起了一次可行的一次性生物传感器的可行替代品的关注,也提供了快速筛选生物分子或生物分子相互作用的前景。在此,在此,我们开发了一种在利用钴(II) - 仲辛酸(NTA)表面化学时成功再生纤维 - 光学(FO)-SPR表面的方法。为了实现这一点,我们测试了多种再生条件,可以在十个再生循环中扰乱与His6标记的抗体片段(SCFV-33H1F7)完全饱和的表面上的NTA螯合物。在将100mM EDTA,500mM咪唑和0.5%SDS在pH 8.0结合1分钟时,在150rpm下振荡,然后用0.5M NaOH洗涤3分钟时,获得最佳表面再生。通过再生NTA表面与三个其他模型系统生物团体进行了10个循环,以其大小和结构不同,证明了既定方法的真正多功能性:HIS6标记的SARS-COV-2穗片段(受体结合域,RBD),a红荧光蛋白(RFP)和蛋白折纸携带4 RFP(TET12SN-RRRR)。能够以快速且成本效益的方式从NTA表面移除His6标记的生物群,可以具有广泛的应用,从生物传感器和各种生物制药分析到新型生物材料的合成。

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