Real-time electrochemical protein monitoring using molecular pendulum sensors
Vuslat Buk JuskaiD, Zhiyuan CheniD, Raza QaziiD, Longshun LiiD, Saehyun KimiD, Fatemeh EsmaeiliiD, Will Buchsbaum, Audrey N. NashneriD, Jane M. DonnellyiD, Luis Fernando Ayala‐CardonaiD, Ryan A. NeffiD, Andrew J. H. SedlackiD, Maria D. CabezasiD, Jagotamoy DasiD, Shana O. KelleyiD, Hossein ZargartalebiiD
Abstract
Continuous monitoring of proteins in complex biological fluids is essential for advancing personalized medicine, yet existing biosensors are often limited by instability, single-use designs, and insufficient sensitivity. Here, we describe a detailed protocol for the fabrication and operation of molecular pendulum (MP) electrochemical sensors integrated with an active-reset mechanism to enable real-time, reversible, and ultrasensitive protein detection. The protocol is described in two parts. First, we describe the microfabrication of gold microelectrodes and their nanostructured modification, followed by assembly of DNA-based pendulum probes with redox reporters and affinity receptors that translate binding into kinetic electron-transfer shifts. Second, we detail the sensing and active-reset approach, which detects the target analyte and applies tunable oscillatory potentials to accelerate its dissociation, regenerate sensor surfaces, and extend operational lifetime. The protocol includes detailed guidance on device fabrication, surface functionalization, sensing and reset cycles, and data analysis. When implemented, MP sensors with active-reset achieve pg/ml sensitivity, rapid equilibration, and robust performance across biofluids and in situ models, enabling continuous protein monitoring over extended periods. This combined technology represents a biosensing platform with significant potential, opening new avenues for wearable and implantable molecular monitoring, early disease detection, and personalized therapeutic guidance.
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