Split aptazyme-based signal amplification for AβO analysis.

Aptazyme is a chimera of functional nucleic acids, which integrates recognition and amplification elements to simplify the assay process and improve sensing efficiency. However, its application may be limited by signal leakage. In this work, we innovatively integrate the AβO aptamer and an MNAzyme (multicomponent nucleic acid enzyme) for highly efficient detection of AβO. The aptamer and half of the MNAzyme are positioned at one strand, and the other half of the MNAzyme is integrated with a toehold sequence. These two sequences cannot hybridize to activate the MNAzyme until the target is added. The background signal is significantly reduced by the split format and the secondary structure of DNA probes formed in the absence of the target. The proposed aptazyme can not only achieve amplification through enzymatic catalysis but also greatly improve the efficiency of signal transduction and output. We systematically investigated the influence of different DNA probes on the detection performance, and the optimized aptazyme can detect as low as 26.5 pM targets in 1h. The stability of this method was also investigated by detection targets in real biological samples. [Display omitted] • A novel aptazyme integrating an aptamer and a well-known MNAzyme (multicomponent DNAzyme) was designed. • The split format is adopted because its more stable in the absence of the target, avoiding signal leakage. • Both the two parts of the aptazyme can form secondary structures to further reduce the background signal. • The detection efficiency is improved by the integration of recognition and signal amplification processes. • The materials used in the method are cost-effective and readily available. [ABSTRACT FROM AUTHOR]