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纳米结构介孔金电极通过电化学信号放大检测癌症中的蛋白质磷酸化。

Nanostructured mesoporous gold electrodes detect protein phosphorylation in cancer with electrochemical signal amplification.

作者信息

Ahmed Emtiaz, Masud Mostafa Kamal, Hossain Md Shahriar A, Na Jongbeom, Sina Abu Ali Ibn, Yamauchi Yusuke, Trau Matt

机构信息

Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD 4072, Australia.

出版信息

Analyst. 2020 Oct 12;145(20):6639-6648. doi: 10.1039/d0an01096k.

Abstract

Protein phosphorylation is a post-translational modification of kinase proteins that changes a protein's conformation to regulate crucial biological functions. However, the phosphorylation of protein is significantly altered during cancer progression which triggers abnormal cellular pathways and this phosphorylation can serve as an emergent diagnostic and prognostic biomarker for cancer. Herein, we develop a nanostructured mesoporous gold electrode (NMGE)-based biosensor that enables a highly sensitive detection of protein phosphorylation with electrochemical signal amplification. The biosensor comprises nanostructured mesoporous gold electrodes whose electro-conductive framework is superior to that of the nonporous electrodes. We characterize our developed nano/mesoporous gold electrode with various electrochemical methods in the presence of the [Fe(CN)6]3-/4- redox system. We find that the mesoporous gold electrode catalyzes both the oxidation and reduction processes of the [Fe(CN)6]3-/4- system and generates a current signal that is 3 times higher than that of the nonporous gold electrode. This superior signal transduction of our nano/mesoporous gold electrode is enabled through a pore-induced (i) high electrochemically active surface area and (ii) reduced impedance with a high signal to noise ratio. The assay utilizes direct adsorption of an immunoprecipitated purified BRAF protein towards the mesoporous gold electrode and thus avoids the cumbersome sensor surface functionalization. Our developed biosensor detects the phosphorylated BRAF protein with a 2.5-fold increase in sensitivity and an ≈10-fold increase in the limit of detection (LOD) in comparison with the nonporous gold electrodes. The assay also works on a wide dynamic range from 0.5 to 20 ng μL-1 of the protein which further shows its potential for clinical application. We envisage that this nanostructured mesoporous gold biosensor will be of high interest for clinical application.

摘要

蛋白质磷酸化是激酶蛋白的一种翻译后修饰,它会改变蛋白质的构象以调节关键的生物学功能。然而,在癌症进展过程中,蛋白质的磷酸化会发生显著变化,从而触发异常的细胞通路,这种磷酸化可作为癌症新出现的诊断和预后生物标志物。在此,我们开发了一种基于纳米结构介孔金电极(NMGE)的生物传感器,该传感器能够通过电化学信号放大实现对蛋白质磷酸化的高灵敏度检测。该生物传感器由纳米结构介孔金电极组成,其导电框架优于无孔电极。我们在[Fe(CN)6]3-/4-氧化还原体系存在的情况下,用各种电化学方法对我们开发的纳米/介孔金电极进行了表征。我们发现介孔金电极催化[Fe(CN)6]3-/4-体系的氧化和还原过程,并产生比无孔金电极高3倍的电流信号。我们的纳米/介孔金电极这种卓越的信号转导是通过孔诱导实现的:(i)具有高电化学活性表面积;(ii)降低了阻抗,具有高信噪比。该检测方法利用免疫沉淀纯化的BRAF蛋白直接吸附到介孔金电极上,从而避免了繁琐的传感器表面功能化。与无孔金电极相比,我们开发的生物传感器检测磷酸化BRAF蛋白的灵敏度提高了2.5倍,检测限(LOD)提高了约10倍。该检测方法在蛋白质浓度为0.5至20 ng μL-1的宽动态范围内也有效,这进一步显示了其临床应用潜力。我们设想这种纳米结构介孔金生物传感器在临床应用中将备受关注。

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