Long Bai, Xiuxiu Wu, Lei Huang, Haohao Chen, Jinsong Yu, Ziqing Ye, Min Yuan, Hui Cao, Liling Hao, Fengqin Yin, Tai Ye, Fei Xu
Aptamer misfolding induced by complex sample matrices often compromises target recognition. Herein, we developed a hydrogel-confinement strategy to stabilize aptamer conformation and effectively suppress matrix interference. Using Pb2+ as a model analyte, aptamers were immobilized during in situ hydrogel polymerization, which helped maintain key binding-related structural features and promoted a G-quadruplex-like pre-organized conformation favorable for target recognition. The confined aptamer acted as a Tb3+ fluorescence sensitizer, enabling label-free Pb2+ detection with an apparent Kd of 0.25 μM and an LOD of 0.4 nM. The optimized aptamer hydrogel, featuring moderate interfacial cationicity and a three-site modified aptamer hydrogel showed 3.1-fold higher affinity than the free aptamer. It maintained stable responses under pH 3, salt concentrations up to 0.5 M, methanol content up to 30%, and nuclease exposure (0.16 U/mL). This strategy was further validated for Cd2+ sensing, demonstrating its potential for aptamer-based detection in complex food and environmental matrices.