Dynamic, Bioresponsive Hydrogels via Changes in DNA Aptamer Conformation

被引:12
作者
Bae, Se Won [1 ,4 ]
Lee, Jae Sung [1 ]
Harms, Victoria M. [1 ]
Murphy, William L. [1 ,2 ,3 ]
机构
[1] Univ Wisconsin, Dept Orthoped & Rehabil, Madison, WI 53792 USA
[2] Univ Wisconsin, Dept Biomed Engn, Madison, WI 53706 USA
[3] Univ Wisconsin, Mat Sci Program, Madison, WI 53706 USA
[4] Korea Inst Ind Technol KITECH, Green Chem & Mat Grp, Cheonan 31056, South Korea
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
aptamers; biomedical applications; DNA; hydrogels; molecular recognition; FUNCTIONALIZED HYDROGEL; RESPONSIVE HYDROGELS; RELEASE; SELECTION; MOLECULES; INSULIN;
D O I
10.1002/mabi.201800353
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA aptamers are integrated into synthetic hydrogel networks with the aim of creating hydrogels that undergo volume changes when exposed to target molecules. Specifically, single-stranded DNA aptamers in cDNA-bound, extended state are incorporated into hydrogel networks as cross-links, so that the nanoscale conformational change of DNA aptamers upon binding to target molecules will induce macroscopic volume decreases of hydrogels. Hydrogels incorporating adenosine triphosphate (ATP)-binding aptamers undergo controllable volume decreases of up to 40.3 +/- 4.6% when exposed to ATP, depending on the concentration of DNA aptamers incorporated in the hydrogel network, temperature, and target molecule concentration. Importantly, this approach can be generalized to aptamer sequences with distinct binding targets, as demonstrated here that hydrogels incorporating an insulin-binding aptamer undergo volume changes in response to soluble insulin. This work provides an example of bioinspired hydrogels that undergo macroscopic volume changes that stem from conformational shifts in resident DNA-based cross-links.
引用
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页数:6
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