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Published July 1, 2022 | Version v1
Journal article

Photoelectrochemical sandwich immunoassay of brain glycogen phosphorylase based on methyl orange–sensitized TiO2 nanorods

  • 1. Hunan Normal University. Key Laboratory of Chemical Biology & Traditional Chinese Medicine Research (Ministry of Education of China), College of Chemistry and Chemical Engineering (China)

Description

The photoelectrochemical immunoassay of glycogen phosphorylase BB (GPBB) was studied. A methyl orange/TiO2 nanorod heterojunction was constructed on a fluorine-doped tin oxide electrode by hydrothermal synthesis, calcination, and chemical adsorption. A sandwich immune structure consisting of GPBB as the first antibody, GPBB, and a CdS@mesoporous silica-ascorbic acid (AA)–GPBB as secondary antibody composite was constructed on each of the selected well surfaces of a 96-well microplate. By adding mercaptoethylamine to structurally destroy the secondary antibody composite and release the electron donor AA, the amplification of photocurrent, and thus the "off–on" photoelectrochemical biosensing of GPBB were realized. The use of the 96-well microplate provides good reproducibility of the assembled immune structures and eliminates the possible effect of the photogenerated hole–induced protein oxidation on the photocurrent. The relevant electrodes and materials were characterized by electrochemistry, UV–vis diffuse reflectance spectra, Fourier transform infrared spectroscopy, X-ray diffractometer, scanning electron microscopy/energy dispersive spectroscopy, transmission electron microscopy and BET method. Under the optimal conditions, the photocurrent was linear with the logarithm of GPBB concentration from 0.005 to 200 ng mL−1 and with a limit of detection of 1.7 pg mL−1 (S/N = 3). Satisfactory results were obtained in the analysis of real serum samples.

Graphical abstract

A sandwich immune structure consisting of GPBB first antibody, GPBB, and a CdS@mesoporous silica-ascorbic acid (AA)–GPBB secondary antibody composite was constructed on each of the selected well surfaces of a 96-well microplate. By adding mercaptoethylamine to structurally destroy the secondary antibody composite and release the electron donor AA, the amplification of photocurrent, and thus the "off–on" photoelectrochemical biosensing of GPBB were realized.

Additional details

Identifiers

Publishing Information

Journal Title
Mikrochimica Acta
Journal Volume
189
Journal Issue
7
Journal Page Range
vp.
ISSN
0026-3672
CODEN
MIACAQ

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Copyright
Copyright (c) 2022 © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2022