学术文献库

This paper presents a dual-aptamer scheme to cancel the signal drifts from structure-switching aptamers during long-term monitoring. Electrochemical aptamer-based (E-AB) biosensors recently demonstrated their great potential for in vivo continuous monitoring. Nevertheless, the detection accuracy is often limited by the signaling drifts. Conventionally, these drifts are removed by the kinetic differential measurements (KDM) when coupled with square-wave voltammetry. Yet we discover that KDM does not apply to every aptamer as the responses at different SWV frequencies heavily depend on its structure-switching characteristics and the redox reporters' electron transfer (ET) kinetics. To this end, we present a "dual-aptamer" scheme that uses two aptamers responding differentially to the same molecular target for drift cancellation. We identify these paired aptamers through (1) screening from the existing aptamers pool and (2) engineering the signaling behavior of the redox reporters. We demonstrate their differential signaling to ampicillin and ATP molecules and show that the aptamer pair bears common drifts in undilute goat serum. Through cancellation, sensor drift is reduced by 370-fold. Benefiting from the "differential" signaling, the recording throughput is also doubled using differential readout electronics. The authors believe the proposed technique is beneficial for long-term in vivo monitoring.