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Application of Bioconjugation Chemistry on Biosensor Fabrication for Detection of TAR-DNA binding Protein 43

机译:生物共轭化学在生物传感器制备中检测TAR-DNA结合蛋白43的应用

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摘要

A simple-prepare, single-use and cost-effective, in vitro biosensor for the detection of TAR DNA-binding protein 43 (TDP-43), a biomarker of neuro-degenerative disorders, was designed, manufactured and tested. This study reports the first biosensor application for the detection of TDP-43 using a novel biosensor fabrication methodology. Bioconjugation mechanism was applied by conjugating anti-TDP 43 with N-succinimidyl S-acetylthioacetate (SATA) producing a thiol-linked anti-TDP 43, which was used to directly link with gold electrode surface, minimizing the preparation steps for biosensor fabrication and simplifying the biosensor surface. The effectiveness of this bioconjugation mechanism was evaluated and confirmed by FqRRM12 protein, using nuclear magnetic resonance (NMR). The surface coverage of the electrode was analyzed by Time-of-Flight-Secondary Ion Mass Spectrometry (TOF-SIMS). Differential pulse voltammetry (DPV) was acted as the detection transduction mechanism with the use of [Fe(CN)6]3−/4-redox probe. Human TDP-43 peptide of 0.0005 μg/mL to 2 μg/mL in undiluted human serum was analyzed using this TDP-43 biosensor. Interference study of the TDP-43 biosensor using β-amyloid 42 protein and T-tau protein confirmed the specifity this TDP-43 biosensor. This bioconjugation chemistry based approach for biosensor fabrication circumvents tedious gold surface modification and functionalization while enabling specific detection of TDP-43 in less than 1 hr with a low fabrication cost of a single biosensor less than $3.
机译:设计,制造和测试了一种简单,一次性且经济高效的体外生物传感器,用于检测TAR DNA结合蛋白43(TDP-43),这是一种神经退行性疾病的生物标记。这项研究报告了首次使用新型生物传感器制造方法检测TDP-43的生物传感器。通过将抗TDP 43与N-琥珀酰亚胺基S-乙酰基硫代乙酸酯(SATA)结合来产生生物缀合机理,从而产生硫醇键合的抗TDP 43,该抗TDP 43可直接与金电极表面连接,从而最大程度地减少了生物传感器的制备步骤并简化了操作生物传感器表面。使用核磁共振(NMR)通过FqRRM12蛋白评估并证实了这种生物偶联机制的有效性。通过飞行时间二次离子质谱分析法(TOF-SIMS)分析电极的表面覆盖率。利用[Fe(CN)6] 3- / 4-redox探针作为差动脉冲伏安法(DPV)。使用该TDP-43生物传感器分析了未稀释的人血清中0.0005μg/ mL至2μg/ mL的人TDP-43肽。使用β-淀粉样蛋白42蛋白和T-tau蛋白对TDP-43生物传感器的干扰研究证实了该TDP-43生物传感器的特异性。这种基于生物共轭化学的生物传感器制造方法可避免繁琐的金表面修饰和功能化,同时能够在不到1小时的时间内对TDP-43进行特异性检测,而单个生物传感器的制造成本却低于3美元。

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