determination-vitro-cellular-turn-on-kinetics-for-fluorogenic-rna

Determination of <em>In Vitro</em> and Cellular Turn-on Kinetics for Fluorogenic RNA Aptamers

Fluorogenic RNA aptamers have been applied in live cells to tag and visualize RNAs, report on gene expression, and activate fluorescent biosensors that ...

University of Utah

In DNA, i-motif (iM) folds occur under slightly acidic conditions when sequences rich in 2'-deoxycytidine (dC) nucleotides adopt consecutive dC self base pairs. The pH stability of an iM is defined by the midpoint in the pH transition (pH ) between the folded and unfolded states. Two different experiments to determine pH values via circular dichroism (CD) spectroscopy were performed on poly-dC iMs of length 15, 19, or 23 nucleotides. These experiments demonstrate two points: (1) pH values were dependent on the titration experiment performed, and (2) pH-induced denaturing or annealing processes produced isothermal hysteresis in the pH values. These results in tandem with model iMs with judicious mutations of dC to thymidine to favor particular folds found the hysteresis was maximal for the shorter poly-dC iMs and those with an even number of base pairs, while the hysteresis was minimal for longer poly-dC iMs and those with an odd number of base pairs. Experiments to follow the iM folding via thermal changes identified thermal hysteresis between the denaturing and annealing cycles. Similar trends were found to those observed in the CD experiments. The results demonstrate that the method of iM analysis can impact the pH parameter measured, and hysteresis was observed in the pH and T values.

Madeline R. Meyer

Department of Chemistry and Henry Eyring Center for Cell & Genome Science

University of Utah

Determination of In Vitro and Cellular Turn-on Kinetics for Fluorogenic RNA Aptamers

Madeline R. Meyer

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Department of Chemistry and Henry Eyring Center for Cell & Genome Science

University of Utah

Determination of In Vitro and Cellular Turn-on Kinetics for Fluorogenic RNA Aptamers

Department of Chemistry and Henry Eyring Center for Cell & Genome Science