Interaction of YOYO-1 with guanine-rich DNA
Source
Journal of Biomolecular Structure and Dynamics
ISSN
07391102
Date Issued
2014-07-03
Author(s)
Abstract
The oxazole homodimer YOYO-1 has served as a valuable tool for the detection and quantification of nucleic acids. While the base specificity and selectivity of binding of YOYO-1 has been researched to some extent, the effect of unorthodox nucleic acid conformations on dye binding has received relatively less attention. In this work, we attempt to correlate the quadruplex-forming ability of G-rich sequences with binding of YOYO-1. Oligonucleotides differing in the number of tandem G repeats, total length, and length of loop sequence were evaluated for their ability to form quadruplexes in presence of sodium (Na<sup>+</sup>) or potassium (K<sup>+</sup>) ions. The fluorescence behavior of YOYO-1 upon binding such G-rich sequences was also ascertained. A distinct correlation was observed between the strength and propensity of quadruplex formation, and the affinity of YOYO-1 to bind such sequences. Specifically, as exemplified by the oligonucleotides 5′-G4T2G4-3′ and 5′-G3TG3TG3-3′, sequences possessing longer G-rich regions and shorter loop sequences formed stronger quadruplexes in presence of K<sup>+</sup> which translated to weaker binding of YOYO-1. The dependence of binding of YOYO-1 on sequence and structural features of G-rich DNA has not been explored previously and such studies are expected to aid in more effective interpretation of applications involving the fluorophore. © 2013 © 2013 Taylor & Francis.
Subjects
fluorescence enhancement of intercalating dyes | G-quadruplex | G-quartet dependence on monovalent cations | nucleic acid staining reagents | quadruplex topology | YOYO-1
