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Updated: Jul 2, 2025

A Flow Cytometry-Based Cell Surface Protein Binding Assay for Assessing Selectivity and Specificity of an Anticancer Aptamer
Published on: September 13, 2022
Quantum measurement enables single biomarker sensitivity in flow cytometry.
J Sabines-Chesterking1,2, I A Burenkov1,2, S V Polyakov3,4
1Joint Quantum Institute, University of Maryland, College Park, 20742, USA.
This study introduces a novel flow cytometry method achieving single-fluorophore sensitivity using quantum principles. It enables precise detection and calibration of individual biomarkers in large cell populations.
Area of Science:
- Quantum Optics
- Biophysics
- Analytical Chemistry
Background:
- Flow cytometry is crucial for analyzing cell populations.
- Current methods often lack single-molecule sensitivity for fluorophores.
- Quantum properties offer new avenues for enhanced detection.
Purpose of the Study:
- To develop an unambiguous experimental method for single-fluorophore sensitivity in flow cytometry.
- To utilize quantum measurements for detecting individual biomarkers.
- To enable precise calibration of flow cytometry measurements.
Main Methods:
- Employing quantum measurement based on the second-order coherence function.
- Utilizing single-photon emitters and their quantum properties.
- Analyzing optical signals from individual biomarkers in a flow cytometer.
Main Results:
- Achieved unambiguous single-fluorophore sensitivity in flow cytometry.
- Demonstrated detection of individual biomarkers using quantum coherence.
- Established a 'photons-to-moles' calibration for the measurement modality.
Conclusions:
- Quantum properties of single-photon emitters enable unprecedented sensitivity in flow cytometry.
- This method allows for rapid detection, enumeration, and sorting of single fluorophores.
- Provides a foundation for advanced biomarker quantification and analysis.
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