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Related Concept Videos

Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

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Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
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Related Experiment Video

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Compact Quantum Dots for Single-molecule Imaging
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Published on: October 9, 2012

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Multi-color single particle tracking with quantum dots.

Eva C Arnspang1, Jonathan R Brewer, B Christoffer Lagerholm

  • 1Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, Odense M, Denmark.

Plos One
|November 17, 2012
PubMed
Summary
This summary is machine-generated.

Quantum dots (QDs) offer advanced fluorescence detection for multiplex single molecule applications. This study quantifies QD properties, enabling multicolor single particle tracking in live cells.

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Area of Science:

  • Nanotechnology
  • Biophysics
  • Spectroscopy

Background:

  • Quantum dots (QDs) offer unique optical properties for sensitive fluorescence detection.
  • Multiplex single molecule applications, like single particle tracking (SPT), require optimized QD performance.
  • Current QD applications have not fully exploited their potential for simultaneous multi-species detection.

Purpose of the Study:

  • To comprehensively investigate fluorescence intensities, fluctuations, and hydrodynamic radii of commercially available water-soluble QDs.
  • To optimize QDs for multiplex single molecule sensitivity applications.
  • To demonstrate multicolor single particle tracking (MC-SPT) with QDs.

Main Methods:

  • Quantitative investigation of eight types of commercially available water-soluble QDs.
  • Analysis of fluorescence intensity, fluorescence intensity fluctuations, and hydrodynamic radii.
  • Demonstration of four-color MC-SPT at an image acquisition rate of 25 Hz.

Main Results:

  • CdSe core QDs show increased fluorescence intensity with red-shifted emission; CdSe/CdTe core QDs are less bright than red-shifted CdSe QDs.
  • Blue-shifted QDs offer minimal size advantage in biological applications due to surface coatings.
  • Parallel four-color MC-SPT is feasible with QDs at >= 25 Hz acquisition rate.

Conclusions:

  • Optimized QDs enable enhanced multiplex single molecule detection.
  • Understanding QD optical and physical properties is crucial for advanced applications.
  • MC-SPT with QDs is a viable technique for studying cellular dynamics in live cells.