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Labeling DNA Probes03:31

Labeling DNA Probes

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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Fluorescence Imaging of Viral Sialidase Activity Using a Fluorogenic Probe.

Tadanobu Takahashi1, Yuuki Kurebayashi2, Tadamune Otsubo3

  • 1Department of Biochemistry, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan. takahasi@u-shizuoka-ken.ac.jp.

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|March 31, 2026
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Summary

Researchers developed novel sialidase imaging probes to visualize viral sialidase activity in infected cells. These probes aid in detecting drug-resistant influenza viruses and understanding viral sialidase localization.

Keywords:
Drug resistanceFluorescence imagingImaging probeInfected cellInfluenza virusNeuraminidaseParamyxovirusSialidase

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Area of Science:

  • Virology
  • Biochemistry
  • Molecular Biology

Background:

  • Influenza and paramyxoviruses possess sialidases that cleave sialic acid, a crucial viral receptor on glycans.
  • Viral sialidase expression is significantly upregulated in cells infected by these viruses.

Purpose of the Study:

  • To develop and characterize novel sialidase imaging probes for visualizing viral sialidase activity.
  • To enable rapid, antibody-free fluorescence imaging of virus-infected cells.
  • To facilitate the detection of drug-resistant influenza strains and study sialidase localization.

Main Methods:

  • Synthesis of a water-soluble, non-fluorescent sialidase imaging probe incorporating sialic acid and a fluorescent moiety.
  • Histochemical visualization of sialidase activity in infected cells using the developed probe.
  • Application of the probe for virus isolation and detection, including drug-resistant strains.

Main Results:

  • The sialidase imaging probe successfully visualized sialidase activity in infected cells.
  • The probe enabled rapid fluorescence imaging without the need for antiviral antibodies or cell fixation.
  • The probe demonstrated utility in detecting drug-resistant influenza viruses and characterizing sialidase localization.

Conclusions:

  • Novel sialidase imaging probes provide an effective tool for visualizing viral sialidase activity.
  • These probes facilitate rapid detection of infected cells and drug-resistant viral strains.
  • The developed probes enhance the study of viral sialidases and their localization.