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Our group uses chemical synthesis,
bottom-up fabrication, and self-assembly to create complex inorganic
nanostructures. The functional
reactivities of magnetic and semiconductor nanoparticles are used as
biomolecular probes, specific targeting, and to exert external forces on
these systems. Our inorganic
nucleic acid mimics are models for multi-electron and energy transfer, which
we apply to complex problems in chemical sensors, molecular electronics, and
artificial photosynthesis.
1. Inorganic DNA: Metal-Linked
Pseudopeptides.
We
have built and studied a new class of biomimetic macromolecules (inorganic
DNA, iDNA), which consist of metal-linked peptide chains. These foundational
investigations demonstrate the creation of artificial peptidic scaffolds that
self-assemble into functional architectures upon metal coordination. As an alternative to
nucleic acid base pairing, our metal chelation binding motif provides a new
strategy for molecular recognition and self-assembly of nanoscale structures.
Modularity of the pseudopeptides allows us to make simple changes in
structure. Our ultimate goal is to build, expand and increase their
complexity for creation of molecular electronic components (diodes, switches,
gain elements), catalytic antennas (multichromophores and catalysts), and sensors
with highly interfaced recognition-dependent electronic and photonic
properties.
The most interesting property of iDNA
structures is that they function as redox systems to experimentally study and
control multi-electron transport. Our structures are distinctive
because the lack of bridging ligands between redox sites means that
multi-electron transfers between weakly coupled metal complexes will
predominantly occur by electron hopping. The arrangement conferred by the
peptide duplexes results in one-dimensional electron hopping frameworks. We
are strategically placed to probe, understand and apply these supramolecular
structures to complex questions of electron transport in multifunctional
arrays.
2. Selective Transport and Placement of
Inorganic Nanoparticles.
Our demonstrated leadership is the product of a multi-faceted
approach that encompasses materials synthesis and analytical methods
development, and application of these to biological systems. Using
magnetotactic bacteria for inspiration, we assemble chemically functional and
magnetic nanoparticles whose solution transport and placement on surfaces is
manipulated with applied magnetic fields or with attached motor
proteins. We were the first group to apply click chemistry to
functionalize nanoparticles; the first to apply field
flow fractionation to the separation of magnetic nanoparticles; and the first to demonstrate control over motor protein
patterning and function with conjugated magnetic nanoparticles. We are
uniquely positioned to make continued advancements at the interface of
magnetic nanoscale materials and biology, where the broader interests include
site-specific drug delivery, magnetic resonance imaging contrast agents, and
separation of complex mixtures.
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