AMPfret: synthetic nanosensor for cellular energy states

Author:

Crocker Hannah1,Pelosse Martin12,Schlattner Uwe23,Berger Imre14ORCID

Affiliation:

1. Bristol Synthetic Biology Centre BrisSynBio, Biomedical Sciences, School of Biochemistry, University of Bristol, 1 Tankard's Close, Bristol BSH 1TD, U.K.

2. Laboratory of Fundamental and Applied Bioenergetics (LBFA) and SFR Environmental and Systems Biology (BEeSy), University of Grenoble Alpes and INSERM U1055, Rue de la Piscine, Domaine Universitaire, Gières 38610, France

3. Institut Universitaire de France (IUF), Paris, France

4. Max Planck Bristol Centre for Minimal Biology, School of Chemistry, Cantock's Close, Bristol BS8 1TS, U.K.

Abstract

Cellular energy is a cornerstone of metabolism and is crucial for human health and disease. Knowledge of the cellular energy states and the underlying regulatory mechanisms is therefore key to understanding cell physiology and to design therapeutic interventions. Cellular energy states are characterised by concentration ratios of adenylates, in particular ATP:ADP and ATP:AMP. We applied synthetic biology approaches to design, engineer and validate a genetically encoded nano-sensor for cellular energy state, AMPfret. It employs the naturally evolved energy sensing of eukaryotic cells provided by the AMP-activated protein kinase (AMPK). Our synthetic nano-sensor relies on fluorescence resonance energy transfer (FRET) to detect changes in ATP:ADP and ATP:AMP ratios both in vitro and in cells in vivo. Construction and iterative optimisation relied on ACEMBL, a parallelised DNA assembly and construct screening technology we developed, facilitated by a method we termed tandem recombineering (TR). Our approach allowed rapid testing of numerous permutations of the AMPfret sensor to identify the most sensitive construct, which we characterised and validated both in the test tube and within cells.

Publisher

Portland Press Ltd.

Subject

Biochemistry

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