化学
适体
体内
微电极
核酸酶
神经化学
生物物理学
多巴胺
生物传感器
电化学
核酸
荧光
组合化学
电化学气体传感器
纳米技术
寡核苷酸
体外
配体(生物化学)
生物化学
作者
Yinghuan Liu,Ying Jin,Fenghui Zhu,X. Li,Chunran Ma,Zhining Sun,Yichun Yao,Kaixin Song,Lanqun Mao,Ying Yan Jiang
摘要
Long-term in vivo neurochemical sensing with aptamer-based electrochemical sensors is fundamentally limited by the enzymatic degradation of natural D-DNA aptamers and the instability of surface-confined sensing interfaces. Here, we generate a mirror-image L-DNA analogue of a dopamine-binding aptamer and show that chiral inversion preserves folding, affinity, and selectivity, as confirmed by circular dichroism, fluorescence binding assays, and molecular docking. Integration of this L-aptamer with a stabilized electrochemical conjugation on carbon-fiber microelectrodes yields a highly stable mirror-image molecular-electrical interface capable of sensitively transducing dopamine binding into quantitative electrochemical signals. Owing to its exceptional nuclease resistance, the L-aptamer sensor enables continuous dopamine monitoring in vivo for over 24 h─an order-of-magnitude improvement in signal over conventional D-aptamer sensors. Applied in Parkinson's disease mouse model, the sensor resolves pathological dopamine clearance defects. These results establish mirror-image nucleic acids, when coupled with engineered electrochemical interfaces, as effective components for durable bioelectronic sensing in vivo.
科研通智能强力驱动
Strongly Powered by AbleSci AI