Rhodamine 6G-Ligand Influencing G-Quadruplex Stability and Topology.

Lukáš Trizna,Andrea Halaganová,Ladislav Janovec,Viktor Víglaský

doi:10.3390/ijms22147639

Lukáš Trizna, Andrea Halaganová + Show 2 more

Open Access

https://doi.org/10.3390/ijms22147639

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Abstract

The involvement of G-quadruplex (G4) structures in nucleic acids in various molecular processes in cells such as replication, gene-pausing, the expression of crucial cancer-related genes and DNA damage repair is well known. The compounds targeting G4 usually bind directly to the G4 structure, but some ligands can also facilitate the G4 folding of unfolded G-rich sequences and stabilize them even without the presence of monovalent ions such as sodium or potassium. Interestingly, some G4-ligand complexes can show a clear induced CD signal, a feature which is indirect proof of the ligand interaction. Based on the dichroic spectral profile it is not only possible to confirm the presence of a G4 structure but also to determine its topology. In this study we examine the potential of the commercially available Rhodamine 6G (RhG) as a G4 ligand. RhG tends to convert antiparallel G4 structures to parallel forms in a manner similar to that of Thiazole Orange. Our results confirm the very high selectivity of this ligand to the G4 structure. Moreover, the parallel topology of G4 can be verified unambiguously based on the specific induced CD profile of the G4-RhG complex. This feature has been verified on more than 50 different DNA sequences forming various non-canonical structural motifs.

Highlights

In this study we investigate the interaction of series of known G4-DNA forming oligonucleotides with rhodamine dyes containing a fluorescent xanthene core; Rhodamine B (RhB) and Rhodamine 6G (RhG)
The so-called (3 + 1) conformer, in which three strands are in the same alignment with another strand oriented in the opposite direction, exhibits a positive shoulder at 265−270 nm, but it should be noted that a mix of parallel and antiparallel structures can show signatures which are close to the topology of (3 + 1) conformers [26,27]
Circular dichroism (CD) spectra can be used for the detection of i-motifs; the maximum and minimum Cotton effects at 288 and 258 nm are indicative of the formation of this structure and the peaks at 275 and 249 nm are indicative of unstructured DNA [30]