光致聚合物
自愈水凝胶
弹性体
材料科学
荧光团
聚合物
聚合
AP站点
甲基丙烯酰胺
单体
丙烯酸酯
DNA
荧光
纳米技术
高分子化学
DNA损伤
化学
复合材料
物理
量子力学
生物化学
丙烯酰胺
作者
Guido Creusen,Ricarda Sophia Schmidt,Andreas Walther
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2021-05-13
卷期号:10 (6): 671-678
被引量:20
标识
DOI:10.1021/acsmacrolett.1c00211
摘要
DNA mechanosensors offer unique properties for mechano-adaptive and self-reporting materials, such as programmable bond strength and geometrical strain response, tunable fluorescent strain sensing, interfacing to biological systems, and the ability to store mechanical information. However, the facile incorporation of advanced DNA motifs into polymer networks and achieving robustness in application settings remain difficult. Herein, we introduce one-component DNA mechanoprobes that can be easily polymerized into polymer hydrogels and even elastomers to allow strain-induced fluorescence sensing. The all-in-one mechanoprobe contains a DNA hairpin for programmable force sensing, an internal fluorophore–quencher pair as a reporter, and methacrylamide groups on both ends for rapid and facile photopolymerization into networks based on the nontoxic water-soluble monomer methoxy triethylene glycol acrylate (mTEGA). In addition to mechanosensing hydrogels, we utilize the low Tg of p(mTEGA) to develop the first bulk elastomer materials with DNA force sensors, which show high elasticity and stronger mechanofluorescence. The system makes decisive steps forward for DNA-based mechanoprobes by overcoming the classical multicomponent design of such probes, allowing photopolymerization useful for the design of complex objects or even 3D printing and demonstrating that such motifs may even be useful in dry bulk materials.
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