Precise detection and dynamic modulation of G-quadruplexes (G4s) are essential for understanding their roles in gene regulation, genome stability, and disease, yet existing ligands often lack topological selectivity or practical applicability. Here, the authors report a π-extended compound, S2, that self-assembles into chiral helical nanoassemblies enabling stereoselective, ratiometric discrimination of G4 topologies. Notably, S2 supported in situ RNA G4 imaging in living cells and quantitative detection in clinical blood samples, differentiating healthy individuals from lung cancer patients.
- Yongxin Chang
- Yiyao Zheng
- Guangyan Qing