Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Participation of the purinergic P2X7 receptor in molecular complexes in the nucleus of human chondrocytes.

Cellular and molecular life sciences : CMLS·2026
Same author

P2X receptors in immune cells: key regulators of inflammation and immune function.

Neuropharmacology·2026
Same author

A bioluminescent ratiometric sensor for the measurement of extracellular ATP concentration in inflammation and cancer.

Neuropharmacology·2026
Same author

In tribute to Francesco Di Virgilio, a great scientist and a wonderful friend.

Purinergic signalling·2026
Same author

The Concise Guide to PHARMACOLOGY 2025/26: Ion channels.

British journal of pharmacology·2025
Same author

Basic Science and Pathogenesis.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2025

Related Experiment Video

Updated: May 9, 2026

Imaging of Intracellular ATP in Organotypic Tissue Slices of the Mouse Brain using the FRET-based Sensor ATeam1.03YEMK
11:20

Imaging of Intracellular ATP in Organotypic Tissue Slices of the Mouse Brain using the FRET-based Sensor ATeam1.03YEMK

Published on: December 19, 2019

Detecting adenosine triphosphate in the pericellular space.

Simonetta Falzoni1, Giovanna Donvito, Francesco Di Virgilio

  • 1Department of Morphology, Surgery and Experimental Medicine, Section of General Pathology , University of Ferrara , Via Borsari 46, Ferrara 44121 , Italy.

Interface Focus
|July 16, 2013
PubMed
Summary

Researchers developed a novel plasma membrane luciferase probe to accurately measure extracellular adenosine triphosphate (ATP) levels. This tool enables sensing ATP in various conditions, including inflammation and tumors.

Keywords:
bioluminescencecancerextracellular adenosine triphosphateinflammationluciferase

More Related Videos

Fluorescence Microscopy for ATP Internalization Mediated by Macropinocytosis in Human Tumor Cells and Tumor-xenografted Mice
08:31

Fluorescence Microscopy for ATP Internalization Mediated by Macropinocytosis in Human Tumor Cells and Tumor-xenografted Mice

Published on: June 30, 2021

Measuring Nucleotide Binding to Intact, Functional Membrane Proteins in Real Time
08:33

Measuring Nucleotide Binding to Intact, Functional Membrane Proteins in Real Time

Published on: March 11, 2021

Related Experiment Videos

Last Updated: May 9, 2026

Imaging of Intracellular ATP in Organotypic Tissue Slices of the Mouse Brain using the FRET-based Sensor ATeam1.03YEMK
11:20

Imaging of Intracellular ATP in Organotypic Tissue Slices of the Mouse Brain using the FRET-based Sensor ATeam1.03YEMK

Published on: December 19, 2019

Fluorescence Microscopy for ATP Internalization Mediated by Macropinocytosis in Human Tumor Cells and Tumor-xenografted Mice
08:31

Fluorescence Microscopy for ATP Internalization Mediated by Macropinocytosis in Human Tumor Cells and Tumor-xenografted Mice

Published on: June 30, 2021

Measuring Nucleotide Binding to Intact, Functional Membrane Proteins in Real Time
08:33

Measuring Nucleotide Binding to Intact, Functional Membrane Proteins in Real Time

Published on: March 11, 2021

Area of Science:

  • Biochemistry
  • Cell Biology
  • Molecular Biology

Background:

  • Extracellular adenosine triphosphate (ATP) plays crucial roles in physiological and pathological processes.
  • Measuring extracellular ATP has been technically challenging.
  • Previous methods for detecting extracellular ATP were limited.

Purpose of the Study:

  • To engineer a reliable biosensor for quantifying extracellular ATP.
  • To develop a tool for monitoring ATP levels in disease models.

Main Methods:

  • Construction of a chimeric protein: firefly luciferase fused with folate receptor leader and anchor sequences.
  • Targeting and expression of the chimeric protein to the plasma membrane outer surface.
  • Generation of stably transfected HEK293 cell clones as ATP sensors.

Main Results:

  • Successfully localized a novel luciferase probe to the plasma membrane outer surface.
  • Developed HEK293 cell clones capable of sensing extracellular ATP concentrations.
  • Demonstrated the utility of the probe in detecting ATP in disease models like tumors and inflammation.

Conclusions:

  • The plasma membrane luciferase probe provides a robust method for measuring extracellular ATP.
  • This engineered biosensor facilitates in vitro and in vivo monitoring of ATP levels.
  • The tool has potential applications in studying ATP's role in various diseases.