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Monitoring Single DNA Docking Site Activity with Sequential Modes of an Optoplasmonic Whispering-Gallery Mode
Narima Eerqing1,2, Ekaterina Zossimova1,3, Sivaraman Subramanian1
1Living Systems Institute, University of Exeter, Exeter EX4 4QD, UK.
Sensors (Basel, Switzerland)
|October 16, 2025
Summary
This study introduces a new method to analyze single DNA molecules on optoplasmonic whispering gallery mode (WGM) sensors. Researchers can now pinpoint specific binding sites and understand their interactions with analyte strands.
Area of Science:
- Nanotechnology
- Biophysics
- Analytical Chemistry
Background:
- Single-molecule techniques offer high precision for studying sub-diffraction limit molecules.
- Optoplasmonic whispering gallery mode (WGM) sensing combines LSPR and WGM for label-free characterization, even at the single-ion level.
- Current methods face challenges in isolating individual binding sites on multiplexed sensors.
Purpose of the Study:
- To characterize distinct binding sites of DNA analyte molecules on an optoplasmonic WGM sensor.
- To differentiate transient interactions from permanent hybridization at specific docking sites.
- To advance the understanding of molecular interactions at the single-molecule level using advanced sensing techniques.
Main Methods:
- Utilized optoplasmonic WGM sensing technology.
- Analyzed DNA hybridization to docking strands on the sensor.
- Employed the ratio of resonance shifts between sequential polar WGM modes for characterization.
Main Results:
- Successfully characterized different binding sites of DNA analyte molecules.
- Identified specific docking sites exhibiting transient interactions.
- Confirmed permanent hybridization of complementary analyte strands at identified sites.
Conclusions:
- The developed method allows for the detailed characterization of individual binding events on optoplasmonic WGM sensors.
- This technique provides insights into the dynamics of molecular interactions, distinguishing transient from stable binding.
- Offers potential for enhanced single-molecule analysis and understanding complex biological processes.
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