Biomod/2012/OSU/OhioMOD: Difference between revisions

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Revision as of 14:59, 27 October 2012

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       <ul>
       <li><a href="#">#Background</a></li>
       <li><a href="#">#Project</a></li>
       <li><a href="#">#Methods</a></li>
       <li><a href="#">#Results</a></li>
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       Triangles are a huge part of the world, as we know it.   They can be found in high strength structures in the form of trusses, woven into spider webs, in the patchwork of a soccer ball, and even in the artwork of Matthew W. Moore.  The versatility of triangles in nature inspired our group to explore their capabilities on the nano scale.  The ultimate goal is to use triangles, combined into parallelograms, as the common factor in the construction of larger, more complex nano structures.  Providing this framework allows for streamlining the formation of various triangle based objects as well as the future ability to shift between various objects via the parallelogram intermediate.
       <br>
       <br>

<b>Abstract:</b><br> Previous DNA origami research has illustrated a wide array of 3D structures. Typically, folding multiple objects requires ordering a new set of DNA components for each desired structure. This project seeks to overcome this limitation by developing a hierarchical assembly framework where multiple 3D shapes can be constructed from a single base DNA origami structure. The basic shape is constructed by folding four equilateral triangles from a single DNA origami scaffold and then arranging them into a parallelogram. Schematics were created to fold these parallelograms into four nanoscale container-like shapes: a tetrahedron, an octahedron, an icosahedron, and a wheel. These final shapes are composed of triangles joined by double stranded DNA connections that can be disrupted utilizing DNA strand displacement to ultimately reconfigure a given shape into a different 3D shape (i.e. reconfigure an octahedron to an icosahedron). This project will enable an economic framework to fabrication of multiple DNA origami structures. Furthermore, this approach could be used to develop DNA structures that can reconfigure in response to a biological stimulus, for example cancer cell microenvironments, for drug delivery applications.

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       <h1>Project</h1>
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       <h1>Methods</h1>
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       <h1>Results/Discussion</h1>
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       <h1>Resources</h1>
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       Castro et. al., A primer to scaffolded DNA origami. Nat Methods 2011; 8(3): 221-220. http://www.ncbi.nlm.nih.gov/pubmed/21358626

<br> Ke et. al., Scaffolded DNA Origami of a DNA Tetrahedron Molecular Container. NanoLett. 2009; 9(6): 2445-2447. http://pubs.acs.org/doi/pdf/10.1021/nl901165f <br> Rothemund et. al., Algorithmic Self-Assembly of DNA Sierpinski Triangles. PLoS Biol. 2004; 2(12): E424. http://www.plosbiology.org/article/info%3Adoi%2F10.1371%2Fjournal.pbio.0020424 <br> Rothemund, Paul W. K. Folding DNA to create nanoscale shapes and patterns. Supplementary Notes 1-11. Nature 2006; 440: 297-302. http://www.nature.com/nature/journal/v440/n7082/extref/nature04586-s1.pdf <br> Rothemund, Paul W. K. Folding DNA to create nanoscale shapes and patterns. Supplementary Note 12. Nature 2006; 440: 297-302. http://www.nature.com/nature/journal/v440/n7082/extref/nature04586-s2.pdf <br> Rothemund, Paul W. K. Folding DNA to create nanoscale shapes and patterns. Nature 2006; 440: 297-302. http://www.nature.com/nature/journal/v440/n7082/full/nature04586.html <br> Wei et. al., Complex shapes self-assembled from single-stranded DNA tiles. Nature 2012; 485: 623-626. http://www.nature.com/nature/journal/v485/n7400/full/nature11075.html <br> Yang et. al., DNA origami with double-stranded DNA as a unified scaffold. ACS Nano. 2012; 6(9): 8209-8215. http://www.ncbi.nlm.nih.gov/pubmed/22830653 <br> Zhao et. al., Organizing DNA origami tiles into larger structures using preformed scaffold frames. Nano Lett. 2011; 11(7): 2997-3002. http://www.ncbi.nlm.nih.gov/pubmed/21682348

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