Good Vibrations Report on the DNA Quadruplex Binding of an Excited State Amplified Ruthenium Polypyridyl IR Probe

• Published in: Journal of the American Chemical Society Vol. 145; no. 39; pp. 21344 - 21360
• Main Authors: Stitch, Mark, Avagliano, Davide, Graczyk, Daniel, Clark, Ian P., González, Leticia, Towrie, Michael, Quinn, Susan J
• Format: Journal Article
• Language: English
• Published: American Chemical Society 04.10.2023
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.3c06099

The nitrile containing Ru­(II)­polypyridyl complex [Ru­(phen)2(11,12-dCN-dppz)]2+ (1) is shown to act as a sensitive infrared probe of G-quadruplex (G4) structures. UV–visible absorption spectroscopy reveals enantiomer sensitive binding for the hybrid htel­(K) and antiparallel htel­(Na) G4s formed by the human telomer sequence d­[AG3(TTAG3)3]. Time-resolved infrared (TRIR) of 1 upon 400 nm excitation indicates dominant interactions with the guanine bases in the case of Λ-1/htel­(K), Δ-1/htel­(K), and Λ-1/htel­(Na) binding, whereas Δ-1/htel­(Na) binding is associated with interactions with thymine and adenine bases in the loop. The intense nitrile transient at 2232 cm–1 undergoes a linear shift to lower frequency as the solution hydrogen bonding environment decreases in DMSO/water mixtures. This shift is used as a sensitive reporter of the nitrile environment within the binding pocket. The lifetime of 1 in D2O (ca. 100 ps) is found to increase upon DNA binding, and monitoring of the nitrile and ligand transients as well as the diagnostic DNA bleach bands shows that this increase is related to greater protection from the solvent environment. Molecular dynamics simulations together with binding energy calculations identify the most favorable binding site for each system, which are in excellent agreement with the observed TRIR solution study. This study shows the power of combining the environmental sensitivity of an infrared (IR) probe in its excited state with the TRIR DNA “site effect” to gain important information about the binding site of photoactive agents and points to the potential of such amplified IR probes as sensitive reporters of biological environments.