The
reprogramming of receptor–ligand interactions affords
an opportunity to direct cells to respond to user-defined external
cues. Although this has often been achieved via the genetic engineering
of receptors, an alternative, nongenetic approach is highly demanded.
In this article, we propose the design of oligonucleotide-based synthetic
switches that feature the ability to reprogram the ligand specificity
of the growth factor receptor. We demonstrated that our synthetic
switches induced growth factor signaling via the formation of the
dynamic complex with specific external cues that would otherwise not
induce the signaling. This chemical approach may be applied to designing
a new class of chemical tools that can control the activities of native
cells and represent smart and safer regenerative drugs.