A DNA/RNA
biosensor capable of single nucleotide variation (SNV)
resolution is highly desirable for drug design and disease diagnosis.
To meet the point-of-care demand, rapid, cost-effective, and accurate
SNV detection is of great significance but still suffers from a challenge.
In this work, a unique nonenzymatic dual-modal (multicolorimetric
and photothermal) visualization DNA biosensor is first proposed for
SNV identification on the basis of an entropy-driven nanomachine with
double output DNAs and coordination etching of anisotropic silver
triangular nanoplates (Ag TNPs). When the target initiates the DNA
nanomachine, the liberated multiple output DNAs can be utilized as
a bridge to produce a superparamagnetic sandwich complex. The incoming
poly-C DNA can coordinate and etch highly active Ag+ ions
at the tips of Ag TNPs, causing a shift in the plasmon peak of Ag
TNPs from 808 to 613 nm. The more target DNAs are introduced, the
more output DNAs are released and thus the more Ag+ ions
are etched. The noticeable color changes of anisotropic Ag TNPs can
be differentiated by “naked eye” and accurate temperature
reading. The programmable DNA nanotechnology and magnetic extraction
grant the high specificity. Also, the SNV detection results can be
self-verified by the two-signal readouts. Moreover, the dual-modal
biosensor has the advantages of portability, cost-effectiveness, and
simplicity. Particularly, the exclusive entropy-driven amplifier liberates
double output DNAs to bridge more poly-C DNAs, enabling the dual-modal
visualization DNA biosensor with improved sensitivity.