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使用组氨酸标签-辣根过氧化物酶功能化纳米共轭物与信号放大免疫测定法检测C反应蛋白

Detection of C-Reactive Protein Using Histag-HRP Functionalized Nanoconjugate with Signal Amplified Immunoassay.

作者信息

Siddiqui Mohd Farhan, Khan Zeeshan Ahmad, Park Seungkyung

机构信息

School of Mechanical Engineering, Korea University of Technology and Education, Cheonan 31253, Korea.

出版信息

Nanomaterials (Basel). 2020 Jun 26;10(6):1240. doi: 10.3390/nano10061240.

Abstract

Ultrasensitive detection of biomarkers is highly significant for disease prognosis and public health treatment. Despite wide acceptance in routine laboratory tests, the conventional enzyme-linked immunosorbent assay (ELISA) has been of limited use for early biomarker detection due to insufficient sensitivity and multiple long incubation time. Several nanoprobes have been introduced to circumvent the limitation, however, rapid, simple, and chemical-free nanoprobe synthesis and sensitive detection methods, particularly for ELISA, are still lacking. In this study, we have synthesized a gold nanoprobe, conjugated with multiple 6X-histidine (6X-his) peptide and nickel-horseradish peroxidase (Ni-HRP), for enhancing the colorimetric signal in ELISA. The developed nanoprobe has been tested for the detection of immunologically significant C-reactive protein (CRP) in ELISA format. The performance of designed probe is validated by testing standard and serum samples, and the detection limit of 32.0 pg/mL with R = 0.98 is confirmed. Furthermore, a comparative analysis of the developed nanoprobe was performed with ELISA developed on conventional guidelines, the proposed immunoassay showed an increase of 12-fold sensitivity for detecting CRP due to the high loading of 6Xhis peptide and binding of multiple Ni-HRP on a gold nanoparticle. Additionally, the proposed assay provides a simple, fast, and cost-efficient (not requiring multiple antibodies) detection of CRP with easy nanoprobe synthesis. Moreover, the developed Histag-HRP functionalized nanoconjugate immunoassay is flexible and can be applied to other biomarkers efficiently by using disease specific antibody.

摘要

生物标志物的超灵敏检测对于疾病预后和公共卫生治疗具有极其重要的意义。尽管传统的酶联免疫吸附测定法(ELISA)在常规实验室检测中已被广泛接受,但由于灵敏度不足和多次长时间孵育,其在早期生物标志物检测中的应用有限。已经引入了几种纳米探针来克服这一限制,然而,仍然缺乏快速、简单且无化学试剂的纳米探针合成方法和灵敏的检测方法,特别是对于ELISA而言。在本研究中,我们合成了一种与多个6X-组氨酸(6X-his)肽和镍-辣根过氧化物酶(Ni-HRP)偶联的金纳米探针,用于增强ELISA中的比色信号。所开发的纳米探针已在ELISA形式下用于检测具有免疫意义的C反应蛋白(CRP)。通过检测标准样品和血清样品验证了设计探针的性能,并确定了检测限为32.0 pg/mL,相关系数R = 0.98。此外,将所开发的纳米探针与按照传统方法开发的ELISA进行了对比分析,结果表明,由于6Xhis肽的高负载量以及多个Ni-HRP在金纳米颗粒上的结合,所提出的免疫测定法在检测CRP时灵敏度提高了12倍。此外,所提出的测定法提供了一种简单、快速且经济高效(不需要多种抗体)的CRP检测方法,并且纳米探针合成容易。此外,所开发的组氨酸标签-HRP功能化纳米共轭免疫测定法具有灵活性,通过使用疾病特异性抗体可有效地应用于其他生物标志物的检测。

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