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Microbial Biosensors01:17

Microbial Biosensors

Microbial biosensors are analytical devices that utilize living microbes to detect specific substances through measurable signals. These devices consist of two main components: biosensing organisms and signal-transducing elements. Biosensing organisms, such as Escherichia coli or Saccharomyces cerevisiae, are typically housed in multiwell plates connected to transducers, enabling rapid, real-time detection of target analytes.Signal Generation MechanismWhen a target analyte—such as...

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Lab-on-Microsphere-FRET-Based Multiplex Sensor Platform.

Vera Kuznetsova1, Viktoria Osipova1, Anton Tkach1

  • 1Center of Information Optical Technology, ITMO University, 197101 Saint Petersburg, Russia.

Nanomaterials (Basel, Switzerland)
|January 20, 2021
PubMed
Summary

This study introduces a novel multiplex assay using polymer microspheres with quantum dots for sensitive biomarker detection. The system utilizes Förster resonance energy transfer for enhanced multiplex analysis of biological samples.

Keywords:
AgInS2FRETcyanine dyesmicrospheressensingternary quantum dotstime-resolved fluorescence spectroscopy

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Area of Science:

  • Materials Science
  • Nanotechnology
  • Biomedical Engineering

Background:

  • Development of advanced sensor systems for multiplex analysis is crucial for detecting biomarkers.
  • Quantum dots (QDs) and polymer microspheres (PMS) offer unique optical properties for assay development.

Purpose of the Study:

  • To develop and investigate a novel multiplex assay model based on polymer microspheres encoded with AIS/ZnS quantum dots.
  • To explore Förster resonance energy transfer (FRET) for multiplexing capabilities in the designed system.

Main Methods:

  • Layer-by-layer deposition technique for preparing QD-encoded PMS.
  • Förster resonance energy transfer (FRET) studies between QDs and cyanine dyes.
  • Time-resolved photoluminescence (PL) measurements to analyze energy transfer dynamics.

Main Results:

  • QD photoluminescence quenching increased with decreased QD-dye distance.
  • Sensitized dye PL intensity showed a maximum at two double polyelectrolyte layers.
  • FRET led to decreased QD PL lifetime and increased dye PL lifetime, enabling multiplexing.

Conclusions:

  • The designed PMS encoded with AIS/ZnS QDs enable multiplexing by wavelength and PL lifetimes.
  • This system holds great potential for developing highly selective and sensitive sensor systems.
  • The assay can be used for multiplex analysis to detect biomarkers in cell lysates and body fluids.