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Multicomponent DNA Polymerization Motor Gels

delete2020-08-09
delete16
PRE
AI
R
Ruohong Shi
J
Joshua Fern
W
Weinan Xu
S
Sisi Jia
Q
Qi Huang
G
Gayatri Pahapale
R
Rebecca Schulman *
D
David H. Gracias *
DOI:10.1002/smll.202002946delete
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Abstract

Abstract

En 中文
Hydrogels with the ability to change shape in response to biochemical stimuli are important for biosensing, smart medicine, drug delivery, and soft robotics. Here, a family of multicomponent DNA polymerization motor gels with different polymer backbones is created, including acrylamide-co-bis-acrylamide (Am-BIS), poly(ethylene glycol) diacrylate (PEGDA), and gelatin-methacryloyl (GelMA) that swell extensively in response to specific DNA sequences. A common mechanism, a polymerization motor that induces swelling is driven by a cascade of DNA hairpin insertions into hydrogel crosslinks. These multicomponent hydrogels can be photopatterned into distinct shapes, have a broad range of mechanical properties, including tunable shear moduli between 297 and 3888 Pa and enhanced biocompatibility. Human cells adhere to the GelMA-DNA gels and remain viable during approximate to 70% volumetric swelling of the gel scaffold induced by DNA sequences. The results demonstrate the generality of sequential DNA hairpin insertion as a mechanism for inducing shape change in multicomponent hydrogels, suggesting widespread applicability of polymerization motor gels in biomaterials science and engineering.
Keywords:
DNA nanotechnology
hydrogels
shape change
soft robotics
tissue engineering
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Johns Hopkins University
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