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Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
Published on: November 25, 2015
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Reversible Loading of Nanoscale Elements on a Multicomponent Supramolecular Polymer System by Using DNA Strand
Willem E M Noteborn1, Victorio Saez Talens1, Roxanne E Kieltyka1
1Department of Supramolecular and Biomaterials Chemistry, Leiden Institute of Chemistry, Leiden University, P. O. Box 9502, 2300 RA, Leiden, The Netherlands.
Chembiochem : a European Journal of Chemical Biology
|August 24, 2017
Summary
This study demonstrates switchable supramolecular polymers using DNA-grafted molecules. DNA-labeled gold nanoparticles can be added or removed on demand, controlling material properties.
Area of Science:
- Supramolecular Chemistry
- Materials Science
- Biomaterials Engineering
Background:
- Nucleic acids offer dynamic properties and orthogonal self-assembly for switchable materials.
- Supramolecular polymers require adaptable building blocks for tunable characteristics.
Purpose of the Study:
- To integrate DNA-grafted molecules into multicomponent supramolecular polymers.
- To demonstrate addressability and switchability of these materials using DNA-functionalized nanoparticles.
Main Methods:
- Synthesis of DNA-grafted squaramide bola-amphiphiles.
- Formation of multicomponent supramolecular polymer systems.
- Addressing with DNA-labeled gold nanoparticles (5 and 15 nm) via sequence complementarity.
- Utilizing DNA-strand displacement for nanoparticle removal and rewriting.
Main Results:
- Successful incorporation of DNA-grafted molecules into supramolecular polymers.
- Demonstrated sequence-specific binding of DNA-labeled gold nanoparticles.
- Achieved on-demand erasure and rewriting of nanoparticles using strand displacement.
Conclusions:
- DNA-grafted molecules enable switchable characteristics in supramolecular polymers.
- This system allows for dynamic control over material properties through external addressing.
- The findings open avenues for responsive and reconfigurable biomaterials.
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