Time-Dependent DNA Origami Denaturation by Guanidinium Chloride, Guanidinium Sulfate, and Guanidinium Thiocyanate

Guanidinium (Gdm) undergoes interactions with both hydrophilic and hydrophobic groups and, thus, is a highly potent denaturant of biomolecular structure. However, our molecular understanding of the interaction of Gdm with proteins and DNA is still rather limited. Here, we investigated the denaturation of DNA origami nanostructures by three Gdm salts, i.e., guanidinium chloride (GdmCl), guanidinium sulfate (Gdm(2)SO(4)), and guanidinium thiocyanate (GdmSCN), at different temperatures and in dependence of incubation time. Using DNA origami nanostructures as sensors that translate small molecular transitions into nanostructural changes, the denaturing effects of the Gdm salts were directly visualized by atomic force microscopy. GdmSCN was the most potent DNA denaturant, which caused complete DNA origami denaturation at 50 degrees C already at a concentration of 2 M. Under such harsh conditions, denaturation occurred within the first 15 min of Gdm exposure, whereas much slower kinetics were observed for the more weakly denaturing salt Gdm(2)SO(4) at 25 degrees C. Lastly, we observed a novel non-monotonous temperature dependence of DNA origami denaturation in Gdm(2)SO(4) with the fraction of intact nanostructures having an intermediate minimum at about 40 degrees C. Our results, thus, provide further insights into the highly complex Gdm-DNA interaction and underscore the importance of the counteranion species.

Automated summary

The study investigated the denaturation of DNA origami nanostructures by different Gdm salts, with guanidinium thiocyanate being the most potent denaturant. The results also revealed a non-monotonous temperature dependence of DNA origami denaturation in guanidinium sulfate, emphasizing the complexity of Gdm-DNA interaction.