Surface Transmon Resonance (STR): a handheld nanogap biosensor for real-time, label-free molecular binding kinetics

Despite the exponential growth of microelectronics driven by Moore’s law over half a century, biosensing has remained largely dominated by optical methods such as fluorescence assays and surface plasmon resonance (SPR). Electronic biosensors, particularly field-effect transistor (FET)-based platforms, have historically faced challenges related to Debye screening and the lack of compact, high-frequency instrumentation necessary for label-free, high-sensitivity measurements in conductive solutions. Here, we present a Surface Transmon Resonance (STR) biosensor, a nanogap-enabled electronic platform that exploits a handheld vector network analyzer (nanoVNA) for real-time, phase-resolved detection of protein-protein interactions. Operating at radio frequencies in the hundreds of MHz range, STR decreases Debye screening limitations and provides an SPR-like readout with significantly reduced cost and footprint compared to benchtop optical systems. By characterizing specific bovine serum albumin (BSA) and anti-BSA binding kinetics, we demonstrate that STR biosensors can quantitatively assess molecular affinity and interaction dynamics, capabilities traditionally reserved for optical gold-standard techniques like SPR. This work positions STR as a compact, scalable, and cost-effective electronic alternative to conventional optical biosensors.

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Publication Details

Journal
npj Biosensing
Published
2026-02-19
DOI
https://doi.org/10.1038/s44328-026-00080-3
Primary Topic
Plasmonic and Surface Plasmon Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Surface Transmon Resonance (STR): a handheld nanogap biosensor for real-time, label-free molecular binding kinetics

Bryan Karekin Chantigian, Sang-Hyun Oh
npj Biosensing
Plasmonic and Surface Plasmon Research
article

Surface Transmon Resonance (STR): a handheld nanogap biosensor for real-time, label-free molecular binding kinetics

Bryan Karekin Chantigian, Sang-Hyun Oh
article en

Abstract

Despite the exponential growth of microelectronics driven by Moore’s law over half a century, biosensing has remained largely dominated by optical methods such as fluorescence assays and surface plasmon resonance (SPR). Electronic biosensors, particularly field-effect transistor (FET)-based platforms, have historically faced challenges related to Debye screening and the lack of compact, high-frequency instrumentation necessary for label-free, high-sensitivity measurements in conductive solutions. Here, we present a Surface Transmon Resonance (STR) biosensor, a nanogap-enabled electronic platform that exploits a handheld vector network analyzer (nanoVNA) for real-time, phase-resolved detection of protein-protein interactions. Operating at radio frequencies in the hundreds of MHz range, STR decreases Debye screening limitations and provides an SPR-like readout with significantly reduced cost and footprint compared to benchtop optical systems. By characterizing specific bovine serum albumin (BSA) and anti-BSA binding kinetics, we demonstrate that STR biosensors can quantitatively assess molecular affinity and interaction dynamics, capabilities traditionally reserved for optical gold-standard techniques like SPR. This work positions STR as a compact, scalable, and cost-effective electronic alternative to conventional optical biosensors.

npj BiosensingVol. 3(1)
University of Minnesota (US)
National Science Foundation, Division of Electrical, Communications and Cyber Systems
Openalex Percentile: Top 51%
Plasmonic and Surface Plasmon Research
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