Department of Orthopedics and Rehabilitation, University of Wisconsin-Madison, Madison, WI, 53792, USA.
Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Macromol Biosci. 2019 Feb;19(2):e1800353. doi: 10.1002/mabi.201800353. Epub 2018 Nov 22.
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.
DNA 适体被整合到合成水凝胶网络中,目的是创建在暴露于靶分子时发生体积变化的水凝胶。具体来说,与 cDNA 结合的单链 DNA 适体以伸展状态被整合到水凝胶网络中作为交联点,因此 DNA 适体与靶分子结合时的纳米级构象变化将诱导水凝胶的宏观体积减小。当暴露于三磷酸腺苷 (ATP) 时,整合了 ATP 结合适体的水凝胶经历可控的体积减小,最大可达 40.3±4.6%,具体取决于整合到水凝胶网络中的 DNA 适体的浓度、温度和靶分子浓度。重要的是,这种方法可以推广到具有不同结合靶标的适体序列,正如这里所示,整合胰岛素结合适体的水凝胶会根据可溶性胰岛素发生体积变化。这项工作提供了一个生物启发的水凝胶的例子,这些水凝胶发生宏观体积变化,其源于驻留基于 DNA 的交联点的构象变化。