Parelius Jonášová Eleonóra, Stokke Bjørn Torger
Biophysics and Medical Technology, Department of Physics, NTNU-Norwegian University of Science and Technology, NO-7491 Trondheim, Norway.
Polymers (Basel). 2020 Jan 26;12(2):268. doi: 10.3390/polym12020268.
Responsive hydrogels featuring DNA as a functional unit are attracting increasing interest due to combination of versatility and numerous applications. The possibility to use nucleic acid analogues opens for further customization of the hydrogels. In the present work, the commonly employed DNA oligonucleotides in DNA-co-acrylamide responsive hydrogels are replaced by Morpholino oligonucleotides. The uncharged backbone of this nucleic acid analogue makes it less susceptible to possible enzymatic degradation. In this work we address fundamental issues related to key processes in the hydrogel response; such as partitioning of the free oligonucleotides and the strand displacement process. The hydrogels were prepared at the end of optical fibers for interferometric size monitoring and imaged using confocal laser scanning microscopy of the fluorescently labeled free oligonucleotides to observe their apparent diffusion and accumulation within the hydrogels. Morpholino-based hydrogels' response to Morpholino targets was compared to DNA hydrogels' response to DNA targets of the same base-pair sequence. Non-binding targets were observed to be less depleted in Morpholino hydrogels than in DNA hydrogels, due to their electroneutrality, resulting in faster kinetics for Morpholinos. The electroneutrality, however, also led to the total swelling response of the Morpholino hydrogels being smaller than that of DNA, since their lack of charges eliminates swelling resulting from the influx of counter-ions upon oligonucleotide binding. We have shown that employing nucleic acid analogues instead of DNA in hydrogels has a profound effect on the hydrogel response.
以DNA作为功能单元的响应性水凝胶,因其多功能性和众多应用的结合而越来越受到关注。使用核酸类似物的可能性为水凝胶的进一步定制开辟了道路。在本工作中,DNA - 共 - 丙烯酰胺响应性水凝胶中常用的DNA寡核苷酸被吗啉代寡核苷酸所取代。这种核酸类似物的不带电荷主链使其不易受到可能的酶促降解影响。在这项工作中,我们探讨了与水凝胶响应中的关键过程相关的基本问题;例如游离寡核苷酸的分配和链置换过程。水凝胶是在光纤末端制备的,用于干涉测量尺寸监测,并使用共聚焦激光扫描显微镜对荧光标记的游离寡核苷酸进行成像,以观察它们在水凝胶中的表观扩散和积累。将基于吗啉代的水凝胶对吗啉代靶标的响应与DNA水凝胶对相同碱基对序列的DNA靶标的响应进行了比较。由于其电中性,观察到非结合靶标在吗啉代水凝胶中的消耗比在DNA水凝胶中少,这导致吗啉代的动力学更快。然而,电中性也导致吗啉代水凝胶的总溶胀响应小于DNA水凝胶,因为它们缺乏电荷消除了寡核苷酸结合时反离子流入引起的溶胀。我们已经表明,在水凝胶中使用核酸类似物而非DNA对水凝胶响应有深远影响。