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首页> 外文期刊>Analytical Sciences >A Novel Gold Nanoprobe for a Simple Electrochemiluminescence Determination of a Prostate-specific Antigen Based on a Peptide Cleavage Reaction
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A Novel Gold Nanoprobe for a Simple Electrochemiluminescence Determination of a Prostate-specific Antigen Based on a Peptide Cleavage Reaction

机译:一种新型金纳骨,用于基于肽切割反应的前列腺特异性抗原测定的简单电荧光测定

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A novel gold nanoprobe for a sensitive and simple determination of a prostate-specific antigen (PSA) was designed on the basis of homogeneous detection and a peptide cleavage reaction. The gold nanoprobe (AuNPs-peptide-Ru1) consisted of a specific peptide tagged with a ruthenium(II) complex (Ru1) and gold nanoparticles (AuNPs) conjugated with the peptide via the strong Au–S bond between the AuNPs surface and the thiol group of the peptide. The electrochemiluminescence (ECL) enzymatic-cleavage-reaction-based bioanalytic system based on homogeneous detection has overcome shortcomings from a complicated fabrication process of traditional electrodes. In the presence of the target PSA, it specifically cleaved the peptide of the AuNPs-peptide-Ru1, and the ECL signal substance (Ru1) part dissociated from AuNPs-peptide-Ru1. This resulted in an increase in the ECL intensity. The ECL biosensor could detect PSA concentrations in the range from 1.0 × 10~(?12) to 1.0 × 10~(?9) g/mL, the detection limit was 4.0 × 10~(?13) g/mL. The assay with the advantages of a simple method for PSA was selective and fast. It is superior to the immunoassay, and is a promising strategy to develop biosensors based on enzymatic cleavage including electrochemistry and optics.
机译:基于均相检测和肽切割反应设计了一种新的金纳孔,用于敏感和简单测定前列腺特异性抗原(PSA)。金纳比亚(AUNP-肽-RU1)由标记用钌(II)复合物(RU1)的特定肽和与肽缀合的金纳米颗粒(AUNP),通过AUNPS表面之间的强AU-S键合和肽的硫醇组。基于均相检测的电化学发光(ECL)酶 - 切割反应的生物分析系统克服了传统电极复杂制造过程的缺点。在靶PSA的存在下,它特异性地切割α-peptide-ru1的肽,以及从AuNPS-肽-RU1离解离的ECL信号物质(RU1)部分。这导致了ECL强度的增加。 ECL生物传感器可以检测从1.0×10〜(Δ12)到1.0×10〜(α9)g / ml的PSA浓度,检测极限为4.0×10〜(?13)g / ml。具有简单方法的优点的测定是选择性和快速的。它优于免疫测定,是一种有前途的策略,可基于酶促切割,包括电化学和光学器件等生物传感器。

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