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Protein delivery: DNA nanostructures and cell-surface targeting
Harvard iGEM August 27, 2006
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The Machine Goal: Future modularized drug delivery target cell protein
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DNA Nanostructures Overview
Can design DNA double helices to stick together and form interesting structures. Dr. Ned Seeman, NYU Dr. William Shih, Harvard Paul Rothemund, Caltech A 1.7-kilobase single-stranded DNA that folds into a nanoscale octahedron WILLIAM M. SHIH, JOEL D. QUISPE & GERALD F. JOYCE
Nature 427, 618ミ621 (2004); doi: /nature02307
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Motivation: Why DNA? Fascinating area of research The power of DNA
Watson-Crick base pairing is enormously strong Self-assembly Highly programmable, designable Specificity - targeting to cells
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Design Details
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Design Details: Scaffolded Oragami
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Design Details: Scaffolded Oragami
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Design Details: Scaffolded Oragami
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Design Details: Positional Control
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Design Details: Positional Control
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Design Details: Positional Control
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Design Details: Positional Control
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Design Details: Positional Control
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Design Details: Positional Control
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Progress Built a number of barrel designs Exciting EM Images
Purifying Nanostructures (nearly there after 1 month of trials)
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Exciting EM Images
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Exciting EM Images
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EM Images (snakes on a grid)
c5.0 barrel (10 nM), 0.7% uranyl formate Appear to be lining up end to end, probably because of the stain Images courtesy Shawn Douglas
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To be continued protease Can a protein be protected from protease if attached inside the box? Lid attachment Lid removal protein protease protein
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Acknowledgements Harvard TFs - Shawn Douglas, Nick Stroustrup, Chris Doucette Harvard advisers - Dr. William Shih, Dr. George Church, Dr. Pamela Silver, Dr. Alain Viel, Dr. Jagesh Shah, Dr. Radhika Nagpal iGEM ambassadors iGEM directors
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