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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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Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
05:37

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Published on: April 4, 2025

Plasmon-controlled fluorescence and single DNA strand sequenching.

Nuriye Akbay1, Krishanu Ray, Mustafa H Chowdhury

  • 1Center for Fluorescence Spectroscopy, University of Maryland at Baltimore, Department of Biochemistry and Molecular Biology, 725 West Lombard Street, Baltimore, MD 21201, USA.

Proceedings of Spie--The International Society for Optical Engineering
|September 13, 2013
PubMed
Summary
This summary is machine-generated.

Metallic nanoparticles significantly boost UV fluorophore emission, enhancing brightness and photostability. This metal-enhanced fluorescence (MEF) effect was observed for UV fluorophores and DNA bases, showing promise for advanced optical applications.

Keywords:
DNA sequenchingfluorescencemetal enhanced fluorescencenanotechnologyplasmon controlled fluorescenceplasmonics

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Area of Science:

  • Plasmonics and Nanophotonics
  • Biophysics and Spectroscopy
  • Materials Science

Background:

  • Metal-enhanced fluorescence (MEF) has been demonstrated using visible and near-infrared (NIR) fluorophores.
  • Metallic nanostructures and nanoparticles alter fluorophore photophysical properties, increasing brightness and photostability.
  • Previous studies focused on visible and NIR wavelengths, leaving UV applications less explored.

Purpose of the Study:

  • To extend MEF studies to ultraviolet (UV) wavelengths.
  • To investigate the enhancement of UV fluorophores, including intrinsic protein fluorescence, using aluminum and platinum nanoparticles.
  • To examine the effect of metallic nanoparticles on the fluorescence intensity of DNA bases and DNA G-quadruplex structures.

Main Methods:

  • Ensemble spectroscopic studies to measure fluorescence.
  • Finite-difference time-domain (FDTD) simulations to model nanoparticle effects on UV fluorophores.
  • Steady-state fluorescence emission measurements on DNA bases and G-quadruplexes on metallic substrates.

Main Results:

  • Aluminum and platinum particles were shown to enhance UV fluorophore emission (300-420 nm), including intrinsic protein fluorescence.
  • FDTD calculations confirmed the plasmonic effects of aluminum nanoparticles on nearby UV emitters.
  • Fluorescence intensities of DNA bases increased 2- to 3-fold, and DNA G-quadruplex fluorescence increased approximately 5-fold on Al and Pt substrates compared to quartz controls.

Conclusions:

  • Metallic nanoparticles, specifically aluminum and platinum, effectively enhance fluorescence in the UV spectrum.
  • MEF principles are applicable to UV fluorophores and biomolecules like DNA bases and G-quadruplexes.
  • This work expands the utility of MEF for UV applications and offers new possibilities for biosensing and imaging.