Authors
Yubo Li, Kefu Liu, Xiaodong Hu, Jing Deng, Wenxian Lan, Hongjuan Xue, Wei Tang, Chunyang Cao
Published in
Nucleic acids research. Volume 54. Issue 13. Jul 03, 2026.
Abstract
Small-molecule stabilization of G-quadruplexes (G4s) has become an active focus in nucleic acid-targeted drug discovery. The mechanisms of the ligands' binding selectivity and biological activities are critical for rational drug design. CX-5461, the first clinically advanced G4-targeting agent, has shown notable efficacy in DNA repair-deficient cancers. Its close analogue MTR-106 also displayed comparable anti-proliferative effects on cancer cells. However, the molecular basis of their interaction with G4s remains elusive. Here, through differential scanning calorimetry, complementary biophysical assays, and solution NMR technique, we probed their recognition modes with G4s. Although both ligands induced stronger thermal stabilization of the parallel G4s, the MYT1L quadruplex-duplex hybrid (QDH) formed the most homogeneous ligand-bound complexes in solution, highlighting the G4-duplex junction as a potential recognition site. Solution structural determination at high resolution demonstrated that both CX-5461 and MTR-106 inserted into the G4-duplex junction pocket. Their rigid polyaromatic scaffolds stacked with the 3'-end G-tetrad of G4, while their flexible side chains extended into the groove of QDH to enable spatial recognition. These findings elucidated the molecular basis of G4 recognition by CX-5461 and MTR-106, and provided a structural framework for the rational development of next-generation G4-targeted therapeutics with improved selectivity and efficacy.
PMID:
42406628
Bibliographic data and abstract were imported from PubMed on 07 Jul 2026.
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