IGEM:Harvard/2006/DNA nanostructures
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< IGEM:Harvard | 2006
Contents |
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 Specs
Container Designs
Design 1 |
Design 2 |
Design 3 |
Design 4 |
Latch Designs
latch1 |
latch2 |
Coding
Existing code
Thrombin-aptamer experiments
Notes
Buffers
- Macaya's and Bock's selection buffer: 20 mM Tris-acetate, pH 7.4, 140 mM NaCl / 5 mM KCl / 1 mM CaCl2 / 1 mM MgCl2
Bibliography
- Schultze P, Macaya RF, and Feigon J. . pmid:8107090.
- Liu Y, Lin C, Li H, and Yan H. . pmid:15945116.
- Li WX, Kaplan AV, Grant GW, Toole JJ, and Leung LL. . pmid:8298130.
- Bock LC, Griffin LC, Latham JA, Vermaas EH, and Toole JJ. . pmid:1741036.
- Macaya RF, Schultze P, Smith FW, Roe JA, and Feigon J. . pmid:8475124.
Presentations
Most recent (Week 3)
Week 2: Original proposal
Working Team Members
- Tiffany Chan (talk)
- Katherine Fifer (talk)
- Valerie Lau (talk)
- Matthew Meisel (talk)
- ...and others are welcome!



