Origami-DNA

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As the antigens NIP and fluoresceine can as well be fused to these oligos, we had found the seemingly perfect tool to present strictly defined two-dimensional antigen-patterns to cells carrying our synthetic receptor system.
As the antigens NIP and fluoresceine can as well be fused to these oligos, we had found the seemingly perfect tool to present strictly defined two-dimensional antigen-patterns to cells carrying our synthetic receptor system.
[[Image:Freiburg2008_Fab_on_Origami_animated.gif|800 px]]
[[Image:Freiburg2008_Fab_on_Origami_animated.gif|800 px]]
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[[Image:Freiburg2008_NIP_arrangement_schematical.jpg]]
==Literature==
==Literature==
*Paul W. K. Rothemund: Nature 440, 297-302 (16 March 2006)
*Paul W. K. Rothemund: Nature 440, 297-302 (16 March 2006)
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Revision as of 20:02, 23 October 2008


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Home

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Project Report

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Safety

CoLABoration

_DNA-Origami



Introduction

Paul Rothemund has discovered that it is possible to shape M13-Phage single-strand-DNA simply adding oligonucleotides that will work as „brackets“ when complementing the long single-strand.
In this way, one can generate for example DNA-squares of a certain size with „nods“ at certain distances. One member of our team, Daniel Hautzinger, has recently finished his diploma-thesis on Origami-DNA and the possibilities of generating patterns on these square surfaces by modifying the oligo-nucleotides that build up the nod-points.
As the antigens NIP and fluoresceine can as well be fused to these oligos, we had found the seemingly perfect tool to present strictly defined two-dimensional antigen-patterns to cells carrying our synthetic receptor system. Freiburg2008 Fab on Origami animated.gif File:Freiburg2008 NIP arrangement schematical.jpg

Literature

  • Paul W. K. Rothemund: Nature 440, 297-302 (16 March 2006)

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