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Related Concept Videos

Protein Dynamics in Living Cells01:19

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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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Regioselective Biolistic Targeting in Organotypic Brain Slices Using a Modified Gene Gun
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Fast spatial-selective delivery into live cells.

Ranhua Xiong1, Claire Drullion2, Peter Verstraelen3

  • 1Laboratory of General Biochemistry and Physical Pharmacy, Faculty of Pharmaceutical Sciences, Ghent University, 9000 Ghent, Belgium; Centre for Nano- and Biophotonics, Faculty of Pharmaceutical Sciences, Ghent University, 9000 Ghent, Belgium.

Journal of Controlled Release : Official Journal of the Controlled Release Society
|October 3, 2017
PubMed
Summary
This summary is machine-generated.

We developed a new method called spatially resolved nanoparticle-enhanced photoporation (SNAP) for precise intracellular delivery of compounds into specific cells. This high-throughput technology enables targeted delivery to cell subpopulations or single cells for research and therapeutics.

Keywords:
Cell-selective deliveryIntracellular deliveryNanoparticlesPulsed laserVapour nanobubbles

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Area of Science:

  • Cell Biology
  • Biotechnology
  • Nanotechnology

Background:

  • Intracellular delivery of compounds is crucial for cell biology and therapeutics.
  • Targeted delivery to specific cell subpopulations or single cells remains a challenge.
  • Existing methods often lack precision and high-throughput capabilities for selective cell manipulation.

Purpose of the Study:

  • To develop an integrated platform for high-throughput, spatially resolved nanoparticle-enhanced photoporation (SNAP).
  • To enable safe and precise intracellular delivery of nanomaterials into selected cell subpopulations or single adherent cells.
  • To demonstrate the utility of SNAP for selective cell labeling and targeted drug delivery applications.

Main Methods:

  • Development of an integrated platform for spatially resolved nanoparticle-enhanced photoporation (SNAP).
  • Utilizing nanomaterials for enhanced photoporation in adherent cells.
  • High-throughput screening and selective targeting of cells based on spatial resolution.

Main Results:

  • SNAP enables safe, intracellular delivery of nanomaterials into selected cell subpopulations, including single cells.
  • Demonstrated selective delivery of a contrast agent into polynucleated keratinocytes for downstream purification.
  • The platform offers flexibility and speed for high-throughput, spatially resolved cell labeling.

Conclusions:

  • SNAP is a powerful tool for precise intracellular delivery in selected cell populations.
  • This technology facilitates downstream purification and functional studies of specific cell types.
  • SNAP holds significant potential for advancing cell biology research and targeted drug delivery strategies.