IGEM:Harvard/2006/DNA nanostructures: Difference between revisions

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==Container Designs==
==Container Designs==
<gallery>
<gallery>
Image:Igemharv06_Katie_Val_cylinder1.gif|[[IGEM:Harvard/2006/Container Design 1|Design 1]]: hexagonal core, separate 1-ply lids
Image:Igemharv06_Katie_Val_cylinder1.gif|[[IGEM:Harvard/2006/Container Design 1|Design 1]]<br>hexagonal core, separate 1-ply lids
Image:Smallcontainer2.jpg|[[IGEM:Harvard/2006/Container Design 2|Design 2]]: hexagonal core, separate 2-ply lids
Image:Smallcontainer2.jpg|[[IGEM:Harvard/2006/Container Design 2|Design 2]]<br>hexagonal core, separate 2-ply lids
Image:Igemharv06_msmrect.png|[[IGEM:Harvard/2006/Container Design 3|Design 3]]: rectangular core, continuous 1-ply lids
Image:Igemharv06_msmrect.png|[[IGEM:Harvard/2006/Container Design 3|Design 3]]<br>rectangular core, continuous 1-ply lids
</gallery>
</gallery>


==Coding==
==Coding==

Revision as of 19:57, 21 June 2006

Project Overview

  • Our goal is to to design and implement molecular containers, which can be dynamically opened and closed by an external stimulus.
  • The containers will be implemented as DNA nanostructures, which afford a significant degree of positional control and chemical versatility.
  • As an initial proof-of-concept, we plan to use our DNA containers to demonstrate controllable activation ("delivery") of anti-thrombin aptamers.
  • We expect that molecular containers could have several interesting scientific and clinical applications, such as
    • Drug and gene delivery
    • Bio-marker scavenging (early detection of biomarkers)
    • Directed evolution (compartmentalized selections)
    • Using multiplexing for combinatorial chemical synthesis
    • Capture and stabilization of multiprotein complexes
    • Protein folding (chaperones)
    • Cell sorting

Container Designs

Coding

Existing code

Original proposal