A magnetic-assisted photoelectrochemical (PEC) and colorimetric
(CL) dual-modal biosensing platform with high precision was established
to monitor prostate-specific antigen (PSA) based on Bi2MoO6 nanosheets (BMO) by coupling the aptamer-guided hybridization
chain reaction (HCR) with the hydrolysate-induced vulcanization reaction
of Bi2MoO6 nanosheets. Upon addition of PSA,
trigger DNA (tDNA) was released by the interaction between the target
analyte and the aptamer and then further hybridized with anchor DNA
(aDNA) conjugated on magnetic beads (MBs). The as-released tDNA initiated
the target-assisted HCR in the presence of two alternating hairpin
sequences (Bio-H1 and Bio-H2) to produce nicked long double-stranded
DNA on the surface of MBs, where numerous alkaline phosphatase (ALP)
enzymes could assemble with MBs through the biotin–avidin reaction,
resulting in the hydrolysis of sodium thiophosphate (TP) to H2S. The as-produced H2S reacted with BMO to form
vulcanized BMO (BMO-S), thus leading to obvious enhanced PEC performance
under visible light with the color change from light yellow to brown.
Having optimized the test conditions, the magnetic-assisted biosensing
system holds a good quantitative diagnosis sensitivity area in a range
of 5.0 pg mL–1–100 ng mL–1 with a calculated detection limit down to 3.5 pg mL–1. Meanwhile, a visual colorimetric assay on basis of the change in
the color of the materials was also realized. Given the exceptional
performance of the constructed biosensor, it may possess great promise
as an advanced bioanalytical tool for practical applications.