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Labeling DNA Probes03:31

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DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
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Specific Labeling of Mitochondrial Nucleoids for Time-lapse Structured Illumination Microscopy
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Organosulfur/Selenium-Based Highly Fluorogenic Molecular Probes for Live-Cell Nucleolus Imaging.

Iswar Chandra Mondal1, Maksym Galkin2,3, Shubham Sharma1

  • 1School of Basic Sciences, Indian Institute of Technology, Mandi, H.P.-175005, India.

Chemistry, an Asian Journal
|February 7, 2022
PubMed
Summary

New fluorescent probes selectively image cell nucleoli. These organoselenium and organosulfur dyes offer high contrast and enhanced emission upon binding to RNA, aiding bioimaging applications.

Keywords:
Conformational DynamicsFluorescent ProbeNucleic AcidNucleolus ImagingOrganochalcogens

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Area of Science:

  • Chemical Biology
  • Molecular Imaging
  • Organic Chemistry

Background:

  • Developing selective fluorescent probes is crucial for advanced bioimaging.
  • Organochalcogen compounds offer unique photophysical properties for sensing applications.
  • Targeting specific cellular components like nucleoli requires tailored probe design.

Purpose of the Study:

  • To develop novel fluorogenic cationic organochalcogens for selective RNA imaging.
  • To investigate the mechanism of enhanced fluorescence upon RNA interaction.
  • To demonstrate the utility of these probes for high-contrast nucleoli bioimaging.

Main Methods:

  • Synthesis of novel organoselenium and organosulfur based fluorescent probes.
  • Evaluation of probe selectivity and photophysical properties in aqueous solutions.
  • Confocal microscopy for high-contrast imaging of cell nucleoli.
  • Multiscale simulation studies to understand structure-interaction relationships.

Main Results:

  • Developed cell-permeable, red-emissive probes with high quantum yield upon RNA binding.
  • Demonstrated selective and high-contrast imaging of cell nucleoli.
  • Simulation studies revealed RNA-induced rotational freezing and planarization enhance fluorescence via intramolecular charge transfer.
  • Identified the impact of heavy-chalcogens on improved emissive properties.

Conclusions:

  • Fluorogenic cationic organochalcogens are effective tools for selective RNA and nucleoli imaging.
  • Probe design incorporating cyclic sidearms and heavy-chalcogens enhances fluorescence and selectivity.
  • These probes offer a promising platform for advanced cellular bioimaging.