A simple
and low-cost fluorescence signal-on sensing strategy has
been developed based on functional nucleic acids (FNAs) via energy
transfer between DNA-templated silver nanoclusters (DNA-AgNCs) and
gold nanorods (GNRs). FNAs were used as highly selective recognition
probes, in which an aptamer was used to detect small molecules represented
by tetracycline, and DNAzyme was used to detect heavy metal ions represented
by Pb2+. The fluorescent DNA-AgNCs were synthesized by
the designed oligonucleotide sequences, which consisted of three parts:
AgNCs synthesis template C6G5C6,
spacer T5, and complementary sequences of the aptamer or
enzyme strand. The difference in electrostatic interactions between
ss/dsDNA and positively charged GNRs leads to energy transfer with
different efficiencies. The analytes represented by tetracycline and
Pb2+ can destroy the dsDNA structure and reduce the energy-transfer
efficiency between DNA-AgNCs and GNRs, thus achieving fluorescence
recovery and a signal-on analytical strategy. This strategy has excellent
specificity and sensitivity with limit of detections of 4.411 nM for
tetracycline and 1.416 nM for Pb2+ and has been successfully
applied to detect tetracycline in milk and Pb2+ in river
water. Using DNA-AgNCs formed in situ as signal probes, this strategy
does not require labels or modifications and can be completed without
complex analytical instruments. Moreover, this strategy can be extended
to detect other targets by replacing FNA sequences. Therefore, it
has promising prospects in the sensitive, simple, and rapid detection
of contaminants in food and environment samples.