posted on 2021-07-02, 12:06authored byBernadette Lechner, Simone Hageneder, Katharina Schmidt, Mark P. Kreuzer, Rick Conzemius, Erik Reimhult, Ivan Barišić, Jakub Dostalek
The
growth of surface-attached single-stranded deoxyribonucleic
acid (ssDNA) chains is monitored in situ using an
evanescent wave optical biosensor that combines surface plasmon resonance
(SPR) and optical waveguide spectroscopy (OWS). The “grafting-from”
growth of ssDNA chains is facilitated by rolling circle amplification
(RCA), and the gradual prolongation of ssDNA chains anchored to a
gold sensor surface is optically tracked in time. At a sufficient
density of the polymer chains, the ssDNA takes on a brush architecture
with a thickness exceeding 10 μm, supporting a spectrum of guided
optical waves traveling along the metallic sensor surface. The simultaneous
probing of this interface with the confined optical field of surface
plasmons and additional more delocalized dielectric optical waveguide
modes enables accurate in situ measurement of the
ssDNA brush thickness, polymer volume content, and density gradients.
We report for the first time on the utilization of the SPR/OWS technique
for the measurement of the RCA speed on a solid surface that can be
compared to that in bulk solutions. In addition, the control of ssDNA
brush properties by changing the grafting density and ionic strength
and post-modification via affinity reaction with complementary short
ssDNA staples is discussed. These observations may provide important
leads for tailoring RCA toward sensitive and rapid assays in affinity-based
biosensors.