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

Author:

Marvin Jonathan S.1ORCID,Kokotos Alexandros C.23,Kumar Mukesh2,Pulido Camila23ORCID,Tkachuk Ariana N.1ORCID,Yao Jocelyn Shuxin1ORCID,Brown Timothy A.1ORCID,Ryan Timothy A.123ORCID

Affiliation:

1. HHMI, Ashburn, VA 20147

2. Department of Biochemistry, Weill Cornell Medicine, New York, NY 10065

3. Aligning Science Across Parkinson’s Collaborative Research Network, Chevy Chase, MD 20815

Abstract

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 F 0 -F 1 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.

Funder

HHS | National Institutes of Health

Aligning Science Across Parkinson's

Michael J. Fox Foundation for Parkinson's Research

Publisher

Proceedings of the National Academy of Sciences

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