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Updated: Jul 16, 2026

Fabrication of Electrochemical-DNA Biosensors for the Reagentless Detection of Nucleic Acids, Proteins and Small Molecules
Published on: June 1, 2011
Nanoconfined biosensor for attomolar molecule detection and recycling via DNA strand displacement
Yonghuan Chen1, Xinru Yue1, Minrui Long1
1College of Chemistry and Materials Science, Guangdong Provincial Key Laboratory of Speed Capability Research, Su Bingtian Center for Speed Research and Training, Jinan University, Guangzhou, 510632, China.
None:
Attomolar-level biomolecular detection remains challenging due to inefficient molecular collisions and weak signal transduction at ultralow concentrations. Here, we introduce a recyclable nanoconfined biosensing platform (ABA@NCBS) for adenosine triphosphate (ATP) detection. This platform integrates a programmable DNA strand displacement reaction (SDR) directly within solid-state nanochannels, establishing a strong coupling between molecular recognition and ion transport. Under nanoconfinement, SDR-induced DNA conformational transitions actively modulate channel geometry and ionic migration pathways, converting molecular recognition into amplified and reversible transmembrane current signals. This confined reaction-transport coupling enables attomolar-level sensitivity (LOD = 83.4 aM) with dual linear response regimes, reflecting a transition in the dominant sensing mechanism across concentration ranges. Moreover, the cascade strand displacement circuit enables multistage logic signal transduction and reversible sensor regeneration. The ABA@NCBS system exhibits stable performance through five detection-regeneration cycles and outstanding anti-interference capability in complex artificial sweat matrices. This work establishes a distinct confined reaction-transport-logic sensing paradigm that goes beyond conventional nanoconfined sensors or SDR-based reversible systems, offering a versatile platform for ultrasensitive biosensing and intelligent molecular signal processing.
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