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Related Concept Videos

Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

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

Updated: May 28, 2026

Measurement of Particle Size Distribution in Turbid Solutions by Dynamic Light Scattering Microscopy
09:16

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Published on: January 9, 2017

Low-coherence dynamic light scattering and its potential for measuring cell dynamics.

Katsuhiro Ishii1, Toshiaki Iwai

  • 1The Graduate School for the Creation of New Photonics Industries, 1955-1 Kurematsucho, Nishi-Ku, Hamamatsu, 4311202, Japan. ishii@gpi.ac.jp

Current Pharmaceutical Biotechnology
|November 2, 2011
PubMed
Summary

Low-coherence dynamic light scattering (LC-DLS) overcomes limitations of conventional dynamic light scattering (DLS) in turbid media. This technique enhances the study of cell dynamics and molecular interactions in complex biological samples.

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Area of Science:

  • Biophysics
  • Cell Biology
  • Photonics

Background:

  • Fluorescence correlation spectroscopy (FCS) and dynamic light scattering (DLS) are vital for studying cellular structures and dynamics.
  • Conventional DLS faces challenges in highly scattering biological media due to multiple scattering effects.
  • Overcoming these limitations is crucial for advancing in vivo cellular analysis.

Purpose of the Study:

  • To review the principles and applications of low-coherence dynamic light scattering (LC-DLS).
  • To highlight LC-DLS's advantages over conventional DLS for biological sample analysis.
  • To demonstrate LC-DLS's capability in measuring dynamics in turbid media.

Main Methods:

  • Theoretical and experimental characterization of LC-DLS properties.
  • Application of LC-DLS to measure diffusion coefficients of macromolecules in turbid media.
  • Utilizing LC-DLS to investigate interparticle and molecular interactions.

Main Results:

  • LC-DLS effectively suppresses multiple scattering, a major limitation in conventional DLS.
  • The technique shows significant potential for measuring cell dynamics in complex biological environments.
  • Successful demonstration of diffusion coefficient measurements and interaction studies using LC-DLS.

Conclusions:

  • LC-DLS offers a robust alternative to conventional DLS for studying dynamics in scattering biological samples.
  • The method provides enhanced potential for analyzing cellular dynamics and molecular interactions.
  • LC-DLS is a promising technique for advancing biophysical and cell biology research.