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基于具有磁核的金纳米壳的前列腺癌标志物糖组学分析的先进阻抗生物传感器配置和检测方案。

Advanced impedimetric biosensor configuration and assay protocol for glycoprofiling of a prostate oncomarker using Au nanoshells with a magnetic core.

机构信息

Institute of Chemistry, Slovak Academy of Sciences, Dubravska cesta 9, Bratislava 845 38, Slovak Republic; Glycanostics Ltd., Dubravska cesta 9, Bratislava 845 38, Slovak Republic.

Institute of Chemistry, Slovak Academy of Sciences, Dubravska cesta 9, Bratislava 845 38, Slovak Republic.

出版信息

Biosens Bioelectron. 2019 Apr 15;131:24-29. doi: 10.1016/j.bios.2019.01.052. Epub 2019 Feb 1.

Abstract

In this paper several advances were implemented for glycoprofiling of prostate specific antigen (PSA), what can be applied for better prostate cancer (PCa) diagnostics in the future: 1) application of Au nanoshells with a magnetic core (MP@silica@Au); 2) use of surface plasmons of Au nanoshells with a magnetic core for spontaneous immobilization of zwitterionic molecules via diazonium salt grafting; 3) a double anti-fouling strategy with integration of zwitterionic molecules on Au surface and on MP@silica@Au particles was implemented to resist non-specific protein binding; 4) application of anti-PSA antibody modified Au nanoshells with a magnetic core for enrichment of PSA from a complex matrix of a human serum; 5) direct incubation of anti-PSA modified MP@silica@Au with affinity bound PSA to the lectin modified electrode surface. The electrochemical impedance spectroscopy (EIS) signal was enhanced 43 times integrating Au nanoshells with a magnetic core compared to the biosensor without them. This proof-of-concept study shows that the biosensor could detect PSA down to 1.2 fM and at the same time to glycoprofile such low PSA concentration using a lectin patterned biosensor device. The biosensor offers a recovery index of 108%, when serum sample was spiked with a physiological concentration of PSA (3.5 ng mL).

摘要

在这项研究中,我们在前列腺特异性抗原(PSA)糖组学分析方面取得了一些进展,这有望为未来更好地诊断前列腺癌(PCa)提供帮助:1)应用具有磁性内核的金纳米壳(MP@silica@Au);2)利用具有磁性内核的金纳米壳的表面等离子体,通过重氮盐接枝实现两性离子分子的自发固定;3)采用双抗污策略,即在 Au 表面和 MP@silica@Au 颗粒上整合两性离子分子,以抵抗非特异性蛋白质结合;4)应用修饰有抗 PSA 抗体的金纳米壳与磁性内核,从人血清的复杂基质中富集 PSA;5)将修饰有抗 PSA 的 MP@silica@Au 直接与亲和结合的 PSA 孵育,以修饰有凝集素的电极表面。与没有金纳米壳的生物传感器相比,整合金纳米壳后电化学阻抗谱(EIS)信号增强了 43 倍。这项概念验证研究表明,该生物传感器可以检测到低至 1.2 fM 的 PSA,并且可以使用图案化的凝集素生物传感器设备对如此低浓度的 PSA 进行糖组学分析。当血清样品中 PSA 的生理浓度(3.5ng/mL)被添加到生物传感器时,其回收率指数为 108%。

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