Genetically encoded manipulation of ATP/ADP ratio in human cells uncovers proteomic and physiological signatures of energy stress
The ability of cells to power energy-demanding processes depends on maintaining the ATP hydrolysis reaction a billion-fold away from equilibrium. Cells respond to alterations in the energy state by sensing changes in the ratio of ATP, ADP, AMP, and inorganic phosphate levels. A key barrier to understanding how this happens is a lack of tools for direct manipulation of the energy state in living cells. Here, we introduce ATPGobble-a genetically encoded tool that hydrolyzes ATP in vivo. ATPGobble increases the metabolic rate, decreases [ATP]/[ADP] and [ATP]/[AMP] ratios, and activates AMPK in human cells. We performed a systematic analysis of proteome and phosphoproteome changes caused by ATPGobble, and found that it remodels cytoskeleton, cell cycle, and translation machinery. Our results establish ATPGobble as a powerful new tool for dissecting the regulatory roles of energy state in living cells.
Authors
- Denis V. Titov (ORCID: https://orcid.org/0000-0001-5677-0651)
- Alex E. Ekvik (ORCID: https://orcid.org/0009-0006-3082-2867)
- Megan M. Kober
Institutions
- University of California, Berkeley (US)
Publication Details
- Journal
- Cell chemical biology
- Published
- 2026-04-01
- DOI
- https://doi.org/10.1016/j.chembiol.2026.03.004
- Primary Topic
- Adenosine and Purinergic Signaling
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Howard Hughes Medical Institute
- American-Scandinavian Foundation
- University of California, Davis
- National Institute of General Medical Sciences
- Diabetes Center, University of California, San Francisco