基于肽的靶标诱导裂解用于测定前列腺特异性抗原的电致化学发光肽基生物传感器。
Electrogenerated chemiluminescence peptide-based biosensor for the determination of prostate-specific antigen based on target-induced cleavage of peptide.
作者信息
Qi Honglan, Li Min, Dong Manman, Ruan Sanpeng, Gao Qiang, Zhang Chengxiao
机构信息
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shaanxi Normal University , Xi'an, Shaanxi 710062, PR China.
出版信息
Anal Chem. 2014 Feb 4;86(3):1372-9. doi: 10.1021/ac402991r. Epub 2014 Jan 24.
A novel electrogenerated chemiluminescence peptide-based biosensor (ECL-PB) for the determination of prostate-specific antigen (PSA) was developed on the basis of target-induced cleavage of a specific peptide within Nafion film incorporated with gold nanoparticles (AuNPs) and ECL emitting species. A specific peptide (CHSSKLQK) was used as a molecular recognition element; tris(2,2'-ripyridine) dichlororuthenium(II) (Ru(bpy)3(2+)) was used as ECL emitting species, and ferrocene carboxylic acid (Fc) was employed as ECL quencher. The ECL-PB biosensor was fabricated by casting the mixture of Nafion and AuNPs onto the surface of glassy carbon electrode to form AuNPs/Nafion film, and then, Ru(bpy)3(2+) was electrostatically adsorbed into the AuNPs/Nafion film; finally, the peptide-tagged with ferrocene carboxylic acid (Fc-peptide) was self-assembled onto the surface of the AuNPs. When PSA was present, it specifically cleaved the Fc-peptide, leading the quencher to leave the electrode and resulting in the increase of the ECL intensity obtained from the resulted electrode in 0.1 M phosphate buffer saline (pH 7.4) containing tri-n-propylamine. The results showed that the increased ECL intensity was directly linear to the logarithm of the concentration of PSA in the range from 5.0 × 10(-12) to 5.0 × 10(-9) g/mL. An extremely low detection limit of 8 × 10(-13) g/mL was achieved because of the signal amplification through AuNPs and the ECL background suppression through Fc as ECL quencher. This work demonstrates that the combination of the direct transduction of peptide cleavage events with the highly sensitive ECL method is a promising strategy for the design of enzymatic cleavage-based ECL biosensors with high sensitivity and selectivity.
基于目标诱导切割包含金纳米粒子(AuNPs)和电化学发光(ECL)发光物质的Nafion膜内特定肽段,开发了一种用于测定前列腺特异性抗原(PSA)的新型基于肽的电化学发光生物传感器(ECL-PB)。使用特定肽(CHSSKLQK)作为分子识别元件;三(2,2'-联吡啶)二氯钌(II)(Ru(bpy)3(2+))用作ECL发光物质,二茂铁羧酸(Fc)用作ECL猝灭剂。通过将Nafion和AuNPs的混合物浇铸到玻碳电极表面以形成AuNPs/Nafion膜来制备ECL-PB生物传感器,然后,Ru(bpy)3(2+)通过静电吸附到AuNPs/Nafion膜中;最后,用二茂铁羧酸标记的肽(Fc-肽)自组装到AuNPs表面。当存在PSA时,它特异性切割Fc-肽,导致猝灭剂离开电极,并使所得电极在含有三正丙胺的0.1 M磷酸盐缓冲盐水(pH 7.4)中获得的ECL强度增加。结果表明,在5.0×10(-12)至5.0×10(-9) g/mL范围内,增加的ECL强度与PSA浓度的对数呈直接线性关系。由于通过AuNPs进行信号放大以及通过Fc作为ECL猝灭剂抑制ECL背景而实现了8×10(-13) g/mL的极低检测限。这项工作表明,将肽切割事件的直接转导与高灵敏度ECL方法相结合是设计具有高灵敏度和选择性的基于酶切割的ECL生物传感器的有前景的策略。