Cathode Photoelectrochemical Paper Device for microRNA Detection Based on Cascaded Photoactive Structures and Hemin/Pt Nanoparticle-Decorated DNA Dendrimers.

Abstract

In this work, a lab-on-paper cathode photoelectrochemical (PEC) sensing platform was constructed for ultrasensitive microRNA-141 (miRNA-141) assay using cascaded multiple photo-active structures as signal generators and hemin/Pt nanoparticle (Pt NP) trunk-branching-decorated DNA dendrimers as signal reinforcers. Specifically, pyramid-like Cu2O was first in situ grown on the Au nanoparticle-functionalized tangled cellulose fibers network, followed by the sensitization of trepang-like BiVO4-Bi2S3 heterostructures, forming the cascaded sensitization structures. Then, the DNA dendrimer was introduced into the photocathode sensing interface by coupling the duplex-specific-nuclease (DSN)-induced target recycling reaction with multiple-branched hybridization chain reaction (MHCR). The programmed target recycling procedures propelled using DSN guaranteed the highly amplified transduction of miRNA-141 to the exposed initiator strand, which triggered the cascaded MHCR accompanied by the formation of the DNA dendrimer with unique trunk-branching structures. Finally, the hemin/Pt NP trunk-branching-decorated DNA dendrimer (HPTD) was acquired by the assembly of Pt NPs and hemin on the trunk and branch, respectively. The resulting HPTD with the synergy catalysis of Pt NPs and hemin could efficiently catalyze the decomposition of H2O2 for in situ generation of O2 as the electron acceptor, leading to an enhanced photocurrent response. Based on the target-dependent photocurrent enhancement, ultrasensitive determination of miRNA-141 was realized with persuasive selectivity, high stability, and excellent reproducibility. Thus, the proposed paper-based cathode PEC sensing platform possessed promising application prospect in clinical miRNA diagnosis.