TY - JOUR
T1 - A General DNA-Gated Hydrogel Strategy for Selective Transport of Chemical and Biological Cargos
AU - Gu, Yuwei
AU - Distler, Max E.
AU - Cheng, Ho Fung
AU - Huang, Chi
AU - Mirkin, Chad A.
N1 - Funding Information:
The authors acknowledge S. H. Petrosko and S. M. Rupich for providing editorial input, and Y. Yang for help with rheological measurements. This material is based upon work supported by the Air Force Office of Scientific Research under awards FA9550-17-1-0348 (oligonucleotide synthesis/purification and DNA-nanoparticle functionalization) and FA9550-18-1-0493 (confocal imaging of transport processes), the National Science Foundation under grant CHE-1709888 (synthesis of small-molecule–DNA hybrids), and the Sherman Fairchild Foundation, Inc. (transport modeling). It was also supported as part of the Center for Bio-Inspired Energy Science, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences under award DE-SC0000989 (synthesis of protein–DNA conjugates). This work made use of instruments of IMSERC at Northwestern University that have received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205), the State of Illinois, and the International Institute for Nanotechnology (IIN). C.H. acknowledges the Chinese Scholarship Council (CSC) for funding support (201906130213).
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/10/20
Y1 - 2021/10/20
N2 - The selective transport of molecular cargo is critical in many biological and chemical/materials processes and applications. Although nature has evolved highly efficient in vivo biological transport systems, synthetic transport systems are often limited by the challenges associated with fine-tuning interactions between cargo and synthetic or natural transport barriers. Herein, deliberately designed DNA-DNA interactions are explored as a new modality for selective DNA-modified cargo transport through DNA-grafted hydrogel supports. The chemical and physical characteristics of the cargo and hydrogel barrier, including the number of nucleic acid strands on the cargo (i.e., the cargo valency) and DNA-DNA binding strength, can be used to regulate the efficiency of cargo transport. Regimes exist where a cargo-barrier interaction is attractive enough to yield high selectivity yet high mobility, while there are others where the attractive interactions are too strong to allow mobility. These observations led to the design of a DNA-dendron transport tag, which can be used to universally modify macromolecular cargo so that the barrier can differentiate specific species to be transported. These novel transport systems that leverage DNA-DNA interactions provide new chemical insights into the factors that control selective cargo mobility in hydrogels and open the door to designing a wide variety of drug/probe-delivery systems.
AB - The selective transport of molecular cargo is critical in many biological and chemical/materials processes and applications. Although nature has evolved highly efficient in vivo biological transport systems, synthetic transport systems are often limited by the challenges associated with fine-tuning interactions between cargo and synthetic or natural transport barriers. Herein, deliberately designed DNA-DNA interactions are explored as a new modality for selective DNA-modified cargo transport through DNA-grafted hydrogel supports. The chemical and physical characteristics of the cargo and hydrogel barrier, including the number of nucleic acid strands on the cargo (i.e., the cargo valency) and DNA-DNA binding strength, can be used to regulate the efficiency of cargo transport. Regimes exist where a cargo-barrier interaction is attractive enough to yield high selectivity yet high mobility, while there are others where the attractive interactions are too strong to allow mobility. These observations led to the design of a DNA-dendron transport tag, which can be used to universally modify macromolecular cargo so that the barrier can differentiate specific species to be transported. These novel transport systems that leverage DNA-DNA interactions provide new chemical insights into the factors that control selective cargo mobility in hydrogels and open the door to designing a wide variety of drug/probe-delivery systems.
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U2 - 10.1021/jacs.1c08114
DO - 10.1021/jacs.1c08114
M3 - Article
C2 - 34614359
AN - SCOPUS:85117453652
SN - 0002-7863
VL - 143
SP - 17200
EP - 17208
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 41
ER -