Physical Society Colloquium
Three-Dimensional DNA Nanostructures: Loading and
Selective Release of Cargo for Biological and Materials Applications
Department of Chemistry McGill University
Three-dimensional structures made of DNA hold the potential to encapsulate and
release drugs, selectively encage nanomaterials, regulate the activity of
proteins and assemble networks for catalysis and biomolecule crystallization.
This talk will describe our research group's synthetic approaches to 3D-DNA
structures, such as DNA cages and nanotubes. These can be accessed with a
minimum number of DNA strands in excellent yields. Their geometry, size,
single- and double-stranded forms, permeability and length can be deliberately
varied. They can be dynamically switched to different internal volumes, and can be ‘opened’ or closed with specific DNA strands. The
size-selective encapsulation of gold nanoparticles and small molecules within
these host structures, and the release of this cargo when specific DNA strands
are added will be shown. We will also describe the use of these cages for the
anisotropic organization of hydrophobic units, thus defining new modes of
protein-inspired interactions. These compact 3D-DNA structures can travel
across the plasma membrane of a number of mammalian cells and result in
efficient gene silencing. The molecules shown here represent a new class of
selective cellular probes and drug delivery tools, and can assist the
development of nucleic acid therapeutic routes.
Selected references:
Science, 2008, 321, 1795; Nature Chem. 2013, 5, 868;
J. Am. Chem. Soc. 2013, 135, 11283; ACS Nano 2013, 7, 3022;
Chem. Sci, 2012, 3, 1980; J. Am. Chem. Soc., 2012, 134, 14382;
J. Am. Chem. Soc., 2012, 134, 4280;
J. Am. Chem. Soc. 2012, 134, 2888;
J. Am. Chem. Soc., 2010, 132, 10212; Nature Chem. 2010, 2, 319;
Nature Chem., 2009, 1, 390;
Nature Nanotech., 2009, 4, 349;
J. Am. Chem. Soc., 2007, 129, 13376.
Friday, April 4th 2014, 15:30
Ernest Rutherford Physics Building, Keys Auditorium (room 112)
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