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Related Experiment Video

Updated: Sep 23, 2025

High-throughput Titration of Luciferase-expressing Recombinant Viruses
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Rapid high-throughput compatible label-free virus particle quantification method based on time-resolved luminescence.

Kari Kopra1, Nazia Hassan1, Emmiliisa Vuorinen1

  • 1Department of Chemistry, University of Turku, Henrikinkatu 2, 20500, Turku, Finland.

Analytical and Bioanalytical Chemistry
|May 17, 2022
PubMed
Summary

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Corrigendum to "Long-term neutralization capacity of vaccine and breakthrough infection induced SARS-CoV-2 specific antibodies against omicron subvariants BA.2, XBB.1.5, and JN.1" [Vaccine 68 (2025) 127894].

Vaccine·2025
This summary is machine-generated.

A new time-resolved luminescence method quantifies virus particles quickly and affordably. This Protein-Probe assay offers a simple way to determine virus counts for diagnostics and vaccine development.

Area of Science:

  • Virology
  • Biotechnology
  • Analytical Chemistry

Background:

  • Viruses pose significant global risks, necessitating accurate quantification for diagnostics and vaccine development.
  • Current virus quantification methods are often complex, costly, and require highly purified samples.
  • Existing assays lack direct virus particle count information.

Purpose of the Study:

  • To develop a simple, cost-effective method for rapid virus particle quantification.
  • To establish a novel assay for determining virus particle counts without extensive purification.
  • To provide a tool for accurate virus enumeration in research and development.

Main Methods:

  • Developed a time-resolved luminescence-based assay using a Eu3+-peptide probe.
  • Implemented a mix-and-measure technique for direct virus particle recognition.
Keywords:
Label-freeProtein-ProbeTime-resolved luminescenceVirus particle quantification

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  • Validated the method across diverse enveloped and non-enveloped viral samples.
  • Main Results:

    • The Protein-Probe method provides virus particle counts in minutes.
    • Achieved over tenfold higher detectability for enveloped viruses compared to non-enveloped viruses.
    • Demonstrated a dynamic range from 5E6 to 3E10 viral particles/mL.
    • Successfully quantified multiple types of enveloped and non-enveloped viruses.

    Conclusions:

    • The developed luminescence assay is a robust and efficient tool for virus particle quantification.
    • This method simplifies virus enumeration, making it accessible for diagnostics and vaccine research.
    • The Protein-Probe assay overcomes limitations of current virus quantification techniques.