Abstract
The guanine-rich telomeric repeats can form G-quadruplexes (G4s) that alter the accessibility of the single-stranded telomeric overhang. In this study, we investigated the effects of Na(+) and K(+) on G4 folding and accessibility through cation introduction and exchange. We combined differential scanning calorimetry (DSC), circular dichroism (CD), and single molecule Förster resonance energy transfer (smFRET) to monitor the stability, conformational dynamics, and complementary strand binding accessibility of G4 formed by single-stranded telomeric DNA. Our data showed that G4 formed through heating and slow cooling in K(+) solution exhibited fewer conformational dynamics than G4 formed in Na(+) solution, which is consistent with the higher thermal stability of G4 in K(+). Monitoring cation exchange with real time smFRET at room temperature shows that Na(+) and K(+) can replace each other in G4. When encountering high K(+) at room or body temperature, G4 undergoes a slow conformational rearrangement process which is mostly complete by 2 h. The slow conformational rearrangement ends with a stable G4 that is unable to be unfolded by a complementary strand. This study provides new insights into the accessibility of G4 forming sequences at different time points after introduction to a high K(+) environment in cells, which may affect how the nascent telomeric overhang interacts with proteins and telomerase.