posted on 2014-10-28, 00:00authored byJoon Soo Park, Nam-In Goo, Dong-Eun Kim
Graphene oxide (GO) adsorbing a fluorophore-labeled
single-stranded
(ss) DNA serves as a sensor system because subsequent desorption of
the adsorbed probe DNA from GO in the presence of complementary target
DNA enhances the fluorescence. In this study, we investigated the
interaction of single- and double-stranded (ds) DNAs with GO by using
a fluorescently labeled DNA probe. Although GO is known to preferentially
interact with ssDNA, we found that dsDNA can also be adsorbed on GO,
albeit with lower affinity. Furthermore, the status of ssDNA or dsDNA
previously adsorbed on the GO surface was investigated by adding complementary
or noncomplementary DNA (cDNA or non-cDNA) to the adsorption complex.
We observed that hybridization occurred between the cDNA and the probe
DNA on the GO surface. On the basis of the kinetics driven by the
incoming additional DNA, we propose a mechanism for the desorption
of the preadsorbed probe DNA from the GO surface: the desorption of
the GO-adsorbed DNA was facilitated following its hybridization with
cDNA on the GO surface; when the GO surface was almost saturated with
the adsorbed DNA, nonspecific desorption dominated the process through
a simple displacement of the GO-adsorbed DNA molecules by the incoming
DNA molecules because of the law of mass action. Our results can be
applied to design appropriate DNA probes and to choose proper GO concentrations
for experimental setups to improve specific signaling in many biosensor
systems based on the GO platform.