On-demand controlled bidirectional DNAzyme path for ultra-sensitive heavy metal ion detection.

A bidirectional self-powered biosensor is constructed for the quasi-simultaneous detection of Pb2+ and Hg2+ based on MoS2@CuS heterostructures as an accelerator and hybridization chain reaction (HCR) as a signal amplification strategy. MoS2@CuS heterostructures significantly facilitate electron transfer between glucose and bioelectrodes, thereby greatly improving the detection signal of self-powered biosensors. This novel biosensor employs the unique sequences of DNAzymes to isolate Pb2+ and Hg2+ by the cleavage effect and thymine (T)-Hg2+-thymine (T) structures, respectively. In the process, Pb2+ cuts the sequence of DNAzyme at the bioanode to trigger glucose oxidation to monitor Pb2+. The as-formed T-Hg2+-T structures activate HCR to reduce [Ru(NH3)6]3+ to detect Hg2+ at the biocathode. It is noteworthy that this biosensor not only realizes Pb2+ or Hg2+ detection in a single-electrode, respectively, but also can quasi-simultaneously detect both Pb2+ and Hg2+ in the bioanode and the biocathode. The novel self-powered biosensor identifies Pb2+ in the range of 106 fM to 10 fM with a limit of detection (LOD) of 3.1 fM and Hg2+ in the range of 106 fM to 1 fM with an LOD of 0.33 fM.