iATPSnFR2: A high-dynamic-range fluorescent sensor for monitoring intracellular ATP

Output Details

Preprint October 18, 2023

Published May 15, 2023

We developed a significantly improved genetically encoded quantitative adenosine triphosphate (ATP) sensor to provide real-time dynamics of ATP levels in subcellular compartments. iATPSnFR2 is a variant of iATPSnFR1, a previously developed sensor that has circularly permuted superfolder green fluorescent protein (GFP) inserted between the ATP-binding helices of the ε-subunit of a bacterial F0-F1 ATPase. Optimizing the linkers joining the two domains resulted in a ~fivefold to sixfold improvement in the dynamic range compared to the previous-generation sensor, with excellent discrimination against other analytes, and affinity variants varying from 4 µM to 500 µM. A chimeric version of this sensor fused to either the HaloTag protein or a suitable spectrally separated fluorescent protein provides an optional ratiometric readout allowing comparisons of ATP across cellular regions. Subcellular targeting the sensor to nerve terminals reveals previously uncharacterized single-synapse metabolic signatures, while targeting to the mitochondrial matrix allowed direct quantitative probing of oxidative phosphorylation dynamics.
Identifier (DOI)
10.1073/pnas.2314604121
Tags
  • Original Research

Meet the Authors

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    Jonathan S. Marvin

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    Alexandros Kokotos, PhD

    Key Personnel: Team De Camilli

    Cornell University

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    Mukesh Kumar

  • Camila Pulido, PhD

    Key Personnel: Team De Camilli

    Weill Cornell Medicine

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    Ariana N. Tkachuk

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    Jocelyn Shuxin Yao

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    Timothy A. Brown

  • Timothy Ryan, PhD

    Co-PI (Core Leadership): Team De Camilli

    Cornell University