A General DNA-Gated Hydrogel Strategy for Selective Transport of Chemical and Biological Cargos

被引:26
作者
Gu, Yuwei [1 ,2 ]
Distler, Max E. [1 ,2 ]
Cheng, Ho Fung [1 ,2 ]
Huang, Chi [1 ,2 ]
Mirkin, Chad A. [1 ,2 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Int Inst Nanotechnol, Evanston, IL 60208 USA
基金
美国国家科学基金会;
关键词
NUCLEAR-PORE COMPLEX; RELEASE; SIZE; MECHANISMS; PRINCIPLES; DIFFUSION; MEMBRANES; HYBRIDS;
D O I
10.1021/jacs.1c08114
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:17200 / 17208
页数:9
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