Abstract

The concentration of wild-type tumour suppressor p53wt in cells and blood has a clinical significance for early diagnosis of some types of cancer. We developed a disposable, label-free, field-effect transistor-based immunosensor (BioFET), able to detect p53wt in physiological buffer solutions, over a wide concentration range. Microfabricated, high-purity gold electrodes were used as single-use extended gates (EG), which avoid direct interaction between the transistor gate and the biological solution. Debye screening, which normally hampers target charge effect on the FET gate potential and, consequently, on the registered FET drain-source current, at physiological ionic strength, was overcome by incorporating a biomolecule-permeable polymer layer on the EG electrode surface. Determination of an unknown p53wt concentration was obtained by calibrating the variation of the FET threshold voltage versus the target molecule concentration in buffer solution, with a sensitivity of 1.5 ± 0.2 mV/decade. The BioFET specificity was assessed by control experiments with proteins that may unspecifically bind at the EG surface, while 100pM p53wt concentration was established as limit of detection. This work paves the way for fast and highly sensitive tools for p53wt detection in physiological fluids, which deserve much interest in early cancer diagnosis and prognosis.

Highlights

  • The transcription factor p53 is considered the most important tumour suppressor for its pivotal role in many cellular processes inducing a number of genes implicated in DNA repair, cell-cycle arrest and apoptosis [1,2]

  • A variety of techniques have been proposed for p53wt protein assay, including, but not limited to, colorimetry, chemiluminescence, electrochemiluminescence, immunochromatography, enzyme-linked immunosorbent assays (ELISA), surface-enhanced Raman spectroscopy (SERS), surface plasmon resonance (SPR), electrochemistry, standard and field-effect transistor (FET) based amperometry [3,4,8,9,10,11,12,13,14,15]

  • We have developed a BioFET for the detection, in physiological-like solution, of the wild-type form of the tumour suppressor p53, whose concentration in cells and blood has a clinical significance for early diagnosis of some types of cancer and other importantly related diseases

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Summary

Introduction

The transcription factor p53 is considered the most important tumour suppressor for its pivotal role in many cellular processes inducing a number of genes implicated in DNA repair, cell-cycle arrest and apoptosis [1,2]. High concentrations of p53wt protein in blood have been correlated to asbestosis, cancer of lungs and mesothelioma, even many years before the malignancy became clinically overt [5,6,7]. P53wt concentration in cells and blood deserves a clinical significance for the early diagnosis of many important diseases. A variety of techniques have been proposed for p53wt protein assay, including, but not limited to, colorimetry, chemiluminescence, electrochemiluminescence, immunochromatography, enzyme-linked immunosorbent assays (ELISA), surface-enhanced Raman spectroscopy (SERS), surface plasmon resonance (SPR), electrochemistry, standard and field-effect transistor (FET) based amperometry [3,4,8,9,10,11,12,13,14,15].

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