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<body>
Nucleic
acid nanostructural design is a powerful tool for constructing complex
assemblies of different shapes that can be addressed with nanometer
resolution. For technological applications DNA origami has to be
functionalized in different ways and at selected positions. We
significantly extend the repertoire of available modifiers by "DNA
origami add-ons", introducing DNA-binding protein domains, which can be
selected from hundreds of modular zinc finger proteins (ZFPs). We
modified DNA origami by site-specific incorporation of binding staples
that contain the recognition site for different ZFPs, thus replacing
the need for chemical modifications with self-assembly. An additional
advantage of using proteins for DNA origami functionalization is the
ability to prepare genetic fusions with variable protein functional
domains. Specific binding of ZFP-fusions to DNA origami was
demonstrated by AFM. Further step towards applications was provided by
the idea and experimental demonstration of vertical DNA origami stacks
that can arrange functionalized DNA origami layers in a defined order,
which increases the density of integration and represents a
technological platform for nanoelectronic components.
<iframe width="853" height="480" src="http://www.youtube.com/embed/zpa1YJXFAuk?rel=0" frameborder="0"
allowfullscreen></iframe>
Goals of the project
- Explore the potential of DNA-binding proteins (zinc finger
proteins - ZFPs) for the versatile and multiple position-specific
addressing on DNA origami.
- Explore the feasibility of preparing vertical DNA origami
stacks using DNA or protein tethers for potential applications.
Achievements
a) We
demonstrated proof of the principle for the use of DNA-binding
protein domains for addressing specific positions on DNA origami
rectangles and introducting selected functional protein domains
b) We
designed and experimentally confirmed formation of verticaly stacked
DNA origami layers
<img style="width: 890px; height: 229px; margin-bottom: 10px;"
alt="" src="http://openwetware.org/images/2/2b/Uvodna.png">
Those results would
not have been possible without solving many smaller challenges:
- Solve in vitro solubility problem of ZFPs, which is
essential for manufacturing protein-derivatized DNA origami. We
achieved this by the addition of GST and MBP domains.We constructed,
expressed and purified 11 different combinations of short and long ZFPs
fused to other protein domains.
- Prepare functional fusions of ZFPs with yellow fluorescent
protein (mCitrine) and Renilla luciferase (RLuc) that can sense the
proximity of their DNA-bound positions up to 10 nm distance and
generate optical signals without external illumination.
- Experimentaly determine the selectivity of long zinc finger
domain chimeras for their DNA origami attachment staples using
AlphaScreen and electrophoretic mobility shift assay (EMSA).
- Design attachment staples for binding ZFP chimeras to DNA
origami.
- Design DNA biding staples for DNA-tethered vertical stacks.
- Prepare and purify twin ZFP protein chimeras as DNA origami
tethers.
Relevance and
applications
Our results provide the
foundation for many real world potential applications.The
ability of DNA origami to fold into almost any desired shape combined
with protein functionality at specific positions represents the perfect
marriage for countless applications. Large number of available DNA
binding protein domains show promise for simultaneous and specific
position-specific addressing of DNA origami.
We expect that ZFP
chimeras will push forward the development of high-tech applications
such as <a
href="http://openwetware.org/wiki/Biomod/2011/Slovenia/BioNanoWizards/applabonchip">lab-on-a-nanochip</a>,
novel types of <a
href="http://openwetware.org/wiki/Biomod/2011/Slovenia/BioNanoWizards/appbiosynthteticcompartments">artificial
biosynthetic organelles</a>, light emitting <a
href="http://openwetware.org/wiki/Biomod/2011/Slovenia/BioNanoWizards/appbiosensors">nanosensors</a>
and many others. We extended DNA origami assemblies into the third
dimension by formation of vertical stacks where the vertical
arrangement is formed based either on DNA or protein tethers. Vertical
stacking of DNA origami allows combinations of differently derivatized
(e.g. metalized, carbon nanotube derivatized) DNA layers for the
formation of various <a
href="http://openwetware.org/wiki/Biomod/2011/Slovenia/BioNanoWizards/appnanoelectronics">nanoelectronic
components</a>, such as nanocapacitors, nanobatteries, ID tags
and other devices with dimensions at the nanoscale.
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