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Related Experiment Video

Updated: Oct 29, 2025

Isolation and Genome Analysis of Single Virions using 'Single Virus Genomics'
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Isolation and Genome Analysis of Single Virions using 'Single Virus Genomics'

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Magnetically Single-Cell Virus Stamping.

Rajib Schubert1

  • 1Research and Early Development, Roche Molecular Systems, Pleasanton, CA, USA. rac0820@gmail.com.

Methods in Molecular Biology (Clifton, N.J.)
|July 6, 2021
PubMed
Summary
This summary is machine-generated.

This study introduces a precise method for targeted virus infection of single cells, enabling better understanding of complex tissues. The technique achieves high success rates for stable genetic modification in just minutes.

Keywords:
Animal cellCultured neuronElectromagnetEnveloped virusLentivirusMagnetic guidanceMagnetic nanoparticleOptical guidanceSingle cell transductionVirus stampingVirus transduction

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Area of Science:

  • Molecular Biology
  • Cell Biology
  • Biotechnology

Background:

  • Viral transduction is crucial for genetic engineering of single cells to study complex tissues.
  • Current viral delivery methods have limitations hindering precise single-cell genetic manipulation.
  • Optically accessible cell monolayers are ideal for developing targeted infection protocols.

Purpose of the Study:

  • To present a precise protocol for targeted virus infection of single cells.
  • To overcome limitations of current viral delivery methods in genetic engineering.
  • To enable efficient and stable transgene expression in single cells.

Main Methods:

  • Developed a protocol for precise, targeted virus infection of single cells in optically accessible monolayers.
  • Utilized lentiviruses (LVs) for genetic manipulation.
  • Demonstrated the technique by stamping cultured Hela cells with LVs.

Main Results:

  • The protocol allows targeted virus infection of single cells in minutes.
  • Achieved stable transgene expression within a few days post-infection.
  • Reported success rates approaching 80% for targeted single-cell infection.

Conclusions:

  • The presented protocol offers a precise and efficient method for single-cell genetic engineering.
  • This technique enhances the understanding of complex tissues through reliable viral transduction.
  • The high success rate and speed make this protocol valuable for various research applications.