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Updated: Sep 2, 2025

Automated System for Single Molecule Fluorescence Measurements of Surface-immobilized Biomolecules
Published on: November 2, 2009
Photocurrent quenching by competitive consumption of surface electron donor and light absorption for immunosensing
Yu Du1, Siqi Yu2, Zhaohui Li3
1State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China; Collaborative Innovation Center for Green Chemical Manufacturing and Accurate Detection, University of Jinan, Jinan, 250022, China.
Abstract:
This work designs a competitive consumption strategy of surface electron donor and light absorption for quenching the photocurrent of ZnSnO3 nanocubes/BiOI nanoarrays/polydopamine (ZnSnO3 NCs/BiOI NAs/PDA) as a photoactive material. This material can be formed on electrode surface by successive coating and deposition to provide a substrate for immobilization of capture antibody, and producing strong photocurrent in the presence of ascorbate acid as a surface electron donor due to the well matching structure of band gaps between ZnSnO3 NCs and BiOI NAs, the excellent light absorption ability and high photo-electron conversion efficiency of BiOI NAs and PDA, and the accelerated electron transfer. Using ascorbate oxidase loaded dopamine-melanin nanosphere (DAM-AAO) as a label of the signal (secondary) antibody, the sandwich-type immunoreaction leads to dual photocurrent quenching of the label through the competitive consumption of ascorbate acid with enzymatic oxidation and the light absorption by DAM nanosphere. Thus, a sensitive "On-Off" photoelectrochemical (PEC) immunosensing method is constructed for the analysis of neuron specific enolase (NSE). The proposed method shows a detection range of 0.1 pg/mL -50 ng/mL and a detection limit of 0.03 pg/mL. The excellent performance and the recovery text demonstrated the practicability of the designed strategy and label in immunoassay of different protein biomarkers.

