Abstract
Docking of a
protein-DNA complex onto a nanopore can provide ample observation time for a detailed
inspection of the complex, enabling collection of biophysical data for
detection, identification, and characterization of the biomolecules. While
docking of a protein-DNA complex onto a biological nanopore has enabled analytic
applications of nanopores including DNA sequencing, the application of the same
principle to solid-state nanopores is tempered by poor understanding of the
docking process. Here, we elucidate the behaviour of individual protein-DNA
complexes docked onto a solid-state nanopore by monitoring the nanopore ionic
current. Repeat docking of monovalent streptavidin-DNA
complexes is found to produce ionic current blockades that fluctuate between
discrete levels within the same current blockade. We elucidate the roles of the protein plug and
the DNA tether in the docking process, finding the docking configurations to
determine the multitude of the current blockade levels whereas the frequency of
the current level switching to be determined by the interactions between the molecules
and the solid-state membrane. Finally, we prove the feasibility of using the
nanopore docking principle for single molecule sensing using solid-state
nanopores by detecting conformational changes of a tethered DNA molecule from a
random coil to an i-motif states.
Supplementary materials
Title
before 2nd submission SI 20180501
Description
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