Abstract

ATP levels may represent fundamental health conditions of cells. However, precise measurement of intracellular ATP levels in living cells is hindered by the lack of suitable methodologies. Here, we developed a novel ATP biosensor termed “BTeam”. BTeam comprises a yellow fluorescent protein (YFP), the ATP binding domain of the ε subunit of the bacterial ATP synthase, and an ATP-nonconsuming luciferase (NLuc). To attain emission, BTeam simply required NLuc substrate. BTeam showed elevated bioluminescence resonance energy transfer efficiency upon ATP binding, resulted in the emission spectra changes correlating with ATP concentrations. By using values of YFP/NLuc emission ratio to represent ATP levels, BTeam achieved steady signal outputs even though emission intensities were altered. With this biosensor, we succeeded in the accurate quantification of intracellular ATP concentrations of a population of living cells, as demonstrated by detecting the slight distribution in the cytosol (3.7–4.1 mM) and mitochondrial matrix (2.4–2.7 mM) within some cultured cell lines. Furthermore, BTeam allowed continuous tracing of cytosolic ATP levels of the same cells, as well as bioluminescent imaging of cytosolic ATP dynamics within individual cells. This simple and accurate technique should be an effective method for quantitative measurement of intracellular ATP concentrations.

Highlights

  • Adenosine 5′-triphosphate (ATP) levels may represent fundamental health conditions of cells

  • We developed a novel genetically encoded ratiometric luminescent ATP biosensor, which is based on bioluminescence resonance energy transfer (BRET) and requires no excitation light

  • We developed a novel BRET-based ATP biosensor, termed BTeam

Read more

Summary

Introduction

ATP levels may represent fundamental health conditions of cells. precise measurement of intracellular ATP levels in living cells is hindered by the lack of suitable methodologies. By using values of YFP/ NLuc emission ratio to represent ATP levels, BTeam achieved steady signal outputs even though emission intensities were altered With this biosensor, we succeeded in the accurate quantification of intracellular ATP concentrations of a population of living cells, as demonstrated by detecting the slight distribution in the cytosol (3.7–4.1 mM) and mitochondrial matrix (2.4–2.7 mM) within some cultured cell lines. BTeam allowed continuous tracing of cytosolic ATP levels of the same cells, as well as bioluminescent imaging of cytosolic ATP dynamics within individual cells This simple and accurate technique should be an effective method for quantitative measurement of intracellular ATP concentrations. The improved methods offer a selection of alternative ATP assays, which provide insights into the dynamics of intracellular ATP These methods still have limitations, including the inability to obtain accurate intracellular ATP levels due to the variable bioluminescence output from Correspondence and requests for materials should be addressed to H.I. (email: imamura@ lif.kyoto-u.ac.jp) www.nature.com/scientificreports/

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call