| Literature DB >> 25892241 |
Takafumi Miyamoto1, Elmer Rho2, Vedangi Sample3, Hiroki Akano4, Masaki Magari4, Tasuku Ueno5, Kirill Gorshkov3, Melinda Chen2, Hiroshi Tokumitsu4, Jin Zhang6, Takanari Inoue7.
Abstract
AMP-activated protein kinase (AMPK), whose activity is a critical determinant of cell health, serves a fundamental role in integrating extracellular and intracellular nutrient information into signals that regulate various metabolic processes. Despite the importance of AMPK, its specific roles within the different intracellular spaces remain unresolved, largely due to the lack of real-time, organelle-specific AMPK activity probes. Here, we present a series of molecular tools that allows for the measurement of AMPK activity at the different subcellular localizations and that allows for the rapid induction of AMPK inhibition. We discovered that AMPKα1, not AMPKα2, was the subunit that preferentially conferred spatial specificity to AMPK, and that inhibition of AMPK activity at the mitochondria was sufficient for triggering cytosolic ATP increase. These findings suggest that genetically encoded molecular probes represent a powerful approach for revealing the basic principles of the spatiotemporal nature of AMPK regulation.Entities:
Mesh:
Substances:
Year: 2015 PMID: 25892241 PMCID: PMC4417068 DOI: 10.1016/j.celrep.2015.03.057
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423