Unfolding rates of 1:1 and 2:1 complex of CX-5461 and c-<i>MYC</i> promoter G-quadruplexes revealed by single-molecule force spectroscopy

作者：Hui Peng, Yashuo Zhang, Qun Luo, Xinyu Wang, Huijuan You · 发表于：Biophysics Reports · 年份：2024 · DOI：10.52601/bpr.2024.240018 · 被引用次数：7 · 研究领域：DNA and Nucleic Acid Chemistry、Force Microscopy Techniques and Applications、Advanced biosensing and bioanalysis techniques

CX-5461, also known as pidnarulex, is a strong G4 stabilizer and has received FDA fast-track designation for BRCA1- and BRCA2- mutated cancers. However, quantitative measurements of the unfolding rates of CX-5461-G4 complexes which are important for the regulation function of G4s, remain lacking. Here, we employ single-molecule magnetic tweezers to measure the unfolding force distributions of c- MYC G4s in the presence of different concentrations of CX-5461. The unfolding force distributions exhibit three discrete levels of unfolding force peaks, corresponding to three binding modes. In combination with a fluorescent quenching assay and molecular docking to previously reported ligand-c- MYC G4 structure, we assigned the ~69 pN peak corresponding to the 1:1 (ligand:G4) complex where CX-5461 binds at the G4’s 5'-end. The ~84 pN peak is attributed to the 2:1 complex where CX-5461 occupies both the 5' and 3'. Furthermore, using the Bell-Arrhenius model to fit the unfolding force distributions, we determined the zero-force unfolding rates of 1:1, and 2:1 complexes to be (2.4 ± 0.9) × 10 −8 s −1 and (1.4 ± 1.0) × 10 −9 s −1 respectively. These findings provide valuable insights for the development of G4-targeted ligands to combat c- MYC -driven cancers.