Related Experiment Video
Updated: Jul 4, 2026

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
Published on: April 4, 2025
G-quadruplex structures of human telomere DNA examined by single molecule FRET and BrG-substitution
Kenji Okamoto1, Yuta Sannohe, Tomoko Mashimo
1Department of Chemistry, Graduate School of Science, Kyoto University, Kitashirakawa-oiwakecho, Sakyo-ku, Kyoto 606-8502, Japan.
Abstract:
The human telomere is known to form the G-quadruplex structure to inhibit the activity of telomerase. Its detailed structure has been of great interest. Recently, two kinds of the parallel-antiparallel hybrid structures have been specified in K(+) solution. However, the G-quadruplex structure is generally thought to be in equilibrium among different structures. Here, we describe the single-pair fluorescence resonance energy transfer (sp-FRET) experiments on telomere samples with bromoguanine (BrG)-substitutions, which control the G-quadruplex structures, at different positions and one without any substitution. The observed FRET distributions were decomposed into five components and the relative population of these components depended on the BrG-substitution positions. In order to consistently explain the variety of conformations, we proposed a novel structural model, the so-called triple-strand-core model. On the basis of this model, the components of the FRET distributions were attributed to the mixed-chair hybrid structures, which were reported recently, and chair-type antiparallel structures, which can be predicted from this model. The FRET efficiencies of these structures were explained in terms of partially broken structures due to steric hindrance and inappropriate capping. This basic model also consistently explains experimental results reported previously. Furthermore, using this model, the folding pathway of the hybrid structures and T-loop formation can be predicted.
Related Concept Videos
Telomeres and Telomerase
Replication in Eukaryotes

