Related Experiment Video
Updated: Jul 19, 2025

09:06
Preparation of DNA-crosslinked Polyacrylamide Hydrogels
Published on: August 27, 2014
14.7K
Swelling characteristics of DNA polymerization gels
Joshua Fern1, Ruohong Shi1, Yixin Liu1
1Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD, 21218, USA. rschulm3@jhu.edu.
Soft Matter
|August 17, 2023
Summary
Researchers tuned DNA polymerization hydrogels
Area of Science:
- Biomaterials Science
- Soft Matter Physics
- Synthetic Biology
Background:
- Biomolecular stimuli-responsive hydrogels are crucial for applications like tissue engineering and soft robotics.
- DNA polymerization gels, featuring polymer backbones and DNA crosslinks, offer tunable swelling via strand displacement.
- Previous work demonstrated their use in programmable, shape-changing gel automata.
Purpose of the Study:
- To systematically investigate how DNA crosslink design/concentration and hairpin trigger properties influence DNA polymerization hydrogel swelling.
- To explore the impact of ionic strength on hydrogel swelling dynamics.
- To examine the effect of hydrogel size and shape on swelling response.
Main Methods:
- Fabrication of DNA polymerization hydrogels with varying DNA crosslink densities and hairpin trigger designs.
- Systematic variation of salt concentration (ionic strength) in the swelling solution.
- Characterization of hydrogel swelling kinetics and equilibrium swelling extent.
- Investigation of swelling behavior across different hydrogel dimensions and geometries.
Main Results:
- Hydrogel swelling rate and extent were significantly altered by DNA crosslink design, concentration, and hairpin trigger characteristics.
- Ionic strength proved to be a critical parameter for tuning swelling, affecting both speed and magnitude.
- Hydrogel size and shape influenced swelling dynamics, with larger or more complex shapes exhibiting different responses.
- A quantitative correlation was established between biochemical parameters and macroscopic material swelling behavior.
Conclusions:
- The swelling response of DNA polymerization hydrogels is highly tunable through biochemical and physical parameters.
- Precise control over hydrogel swelling can be achieved by adjusting DNA crosslink/trigger design and ionic strength.
- These findings enable the rational design of DNA polymerization hydrogels for advanced applications in biomimetic materials and soft robotics.
Related Concept Videos
DNA Agarose Gel Electrophoresis
97.2K
Agarose gel electrophoresis is a laboratory technique commonly used to separate DNA fragments by size. However, it can also be used to isolate and purify DNA fragments using a gel extraction protocol.
Gel extraction follows five major steps: running gel electrophoresis to separate fragments, isolating the individual bands, extracting DNA from those bands, and removing the dye and salts from the extracted mixture to obtain pure DNA.
In cloning experiments, both the insert and vector DNA...
Gel extraction follows five major steps: running gel electrophoresis to separate fragments, isolating the individual bands, extracting DNA from those bands, and removing the dye and salts from the extracted mixture to obtain pure DNA.
In cloning experiments, both the insert and vector DNA...
97.2K
Molecular Weight of Step-Growth Polymers
2.2K
Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
2.2K

