The AMP-activated protein kinase (AMPK) acts as a sensor of cellular energy status. AMPK exists as heterotrimeric complexes comprising a catalytic α subunit and regulatory β and γ subunits. In mammals, each of these subunits is encoded by multiple genes and at least 12 possible combinations of subunit isoforms are possible. The α subunits (α1, α2) contain the kinase domain at the N-terminus followed by a C-terminal region that is required for formation of the αβγ complex. The β subunits (β1, β2) contain short, variable N-terminal regions followed by two more highly conserved regions. The first is now recognized to be a glycogen-binding domain (related to N-isoamylase domains that are found in enzymes that metabolize the α1->6 branches in α1->4 linked glucans such as glycogen) that causes AMPK to associate with glycogen particles inside the cell. The C-terminal conserved region is required for the formation of the αβγ complex. The γ subunit isoforms (γ1, γ2, γ3) contain variable N-terminal regions of unknown function, followed by four tandem repeats of a sequence termed a CBS motif. These motifs, which also occur in a small number of other proteins, act in pairs to form two domains that bind the regulatory nucleotides, AMP and ATP, in a mutually exclusive manner. Binding of AMP to the two sites is highly co-operative. Mutations within the AMP binding sites of the γ2 and γ3 isoforms cause glycogen storage disorders in cardiac muscle in humans and skeletal muscle in pigs, respectively.

The AMPK system is activated by cellular stresses that cause a drop in the cellular ATP:ADP ratio either by interfering with ATP synthesis (e.g. metabolic poisons, hypoxia, glucose starvation) or by increasing ATP consumption (e.g. contraction in muscle). An increase in the cellular ADP:ATP ratio is amplified into a much larger increase in AMP:ATP by adenylate kinase. AMP binds to the two sites on the γ subunit (an effect antagonized by high ATP). This promotes phosphorylation within the α subunit by the upstream kinase, which is essential for AMPK activity. The major form of the upstream kinase is a complex between the tumor suppressor LKB1, and two accessory subunits, STRAD and MO25. AMP binding also allosterically activates the phosphorylated AMPK complex. Dissociation of AMP both reverses the allosteric activation and also promotes dephosphorylation to switch the kinase off again.

Once activated, AMPK switches on catabolic processes that generate ATP, such as the uptake and oxidation of glucose and fatty acids. It also switches off processes that consume ATP that are not essential for the short-term survival of the cell. This includes the biosynthesis of fatty acids, cholesterol, glycogen and protein. AMPK switches off protein biosynthesis and cell growth in part by down-regulating the TOR (target-of-rapamycin) pathway. AMPK causes both short-term effects via direct phosphorylation of metabolic enzymes, and longer-term effects by modulating gene expression.

AMPK is a prime target for drugs aimed at treatment of obesity and Type 2 diabetes. It can be activated in intact cells and in vivo using the nucleoside 5-aminoimidazole-4-carboxamide riboside (AICAR), which is taken up by cells and converted to the equivalent monophosphorylated nucleotide, ZMP, which mimics all of the effects of AMP. AMPK is also activated in intact cells and/or in vivo by two major classes of anti-diabetic drugs, i.e. the biguanides (metformin and phenformin) and the thiazolidinediones (rosiglitazone and pioglitazone). These drugs appear to act indirectly on AMPK, possibly via inhibition of the respiratory chain, and it remains uncertain to what extent their therapeutic benefits are mediated by AMPK.

The Table below contains accepted modulators and additional information. For a list of additional products, see the "Similar Products" section below.


a) These activators only work in intact cells and require an intact αβγ complex

b) Compound C may inhibit the isolated kinase domain of the α subunit but has only been tested on the intact αβγ complex; see Zhou, et al., J. Clin. Invest., 108, 1167-1174 (2001).



CHEUNG PCF, SALT IP, DAVIES SP, HARDIE DG, CARLING D. 2000. Characterization of AMP-activated protein kinase ?-subunit isoforms and their role in AMP binding. 346(3):659-669.
Giordanetto F, Karis D. 2012. Direct AMP-activated protein kinase activators: a review of evidence from the patent literature. Expert Opinion on Therapeutic Patents. 22(12):1467-1477.
Hardie D, Scott JW, Pan DA, Hudson ER. 2003. Management of cellular energy by the AMP-activated protein kinase system. 546(1):113-120.
Hardie DG. 2004. The AMP-activated protein kinase pathway - new players upstream and downstream. Journal of Cell Science. 117(23):5479-5487.
Hardie D, Ross F, Hawley S. 2012. AMP-Activated Protein Kinase: A Target for Drugs both Ancient and Modern. Chemistry & Biology. 19(10):1222-1236.
Hardie DG, Ross FA, Hawley SA. 2012. AMPK: a nutrient and energy sensor that maintains energy homeostasis. Nat Rev Mol Cell Biol. 13(4):251-262.
Hawley SA, Boudeau J, Reid JL, Mustard KJ, Udd L, Mäkelä TP, Alessi DR, Hardie DG. 2003. J Biol. 2(4):28.
Hudson ER, Pan DA, James J, Lucocq JM, Hawley SA, Green KA, Baba O, Terashima T, Hardie D. 2003. A Novel Domain in AMP-Activated Protein Kinase Causes Glycogen Storage Bodies Similar to Those Seen in Hereditary Cardiac Arrhythmias. Current Biology. 13(10):861-866.
Inoki K, Zhu T, Guan K. 2003. TSC2 Mediates Cellular Energy Response to Control Cell Growth and Survival. Cell. 115(5):577-590.
O'Neill LAJ, Hardie DG. 2013. Metabolism of inflammation limited by AMPK and pseudo-starvation. Nature. 493(7432):346-355.
Salminen A, Kaarniranta K, Haapasalo A, Soininen H, Hiltunen M. 2011. AMP-activated protein kinase: a potential player in Alzheimer?s disease. 118(4):460-474.
Scott JW, Hawley SA, Green KA, Anis M, Stewart G, Scullion GA, Norman DG, Hardie DG. 2004. CBS domains form energy-sensing modules whose binding of adenosine ligands is disrupted by disease mutations. J. Clin. Invest.. 113(2):274-284.
Scott JW, Norman DG, Hawley SA, Kontogiannis L, Hardie D. 2002. Protein kinase substrate recognition studied using the recombinant catalytic domain of AMP-activated protein kinase and a model substrate. Journal of Molecular Biology. 317(2):309-323.
Stapleton D, Mitchelhill KI, Gao G, Widmer J, Michell BJ, Teh T, House CM, Fernandez CS, Cox T, Witters LA, et al. 1996. Mammalian AMP-activated Protein Kinase Subfamily. J. Biol. Chem.. 271(2):611-614.
Thornton C, Snowden MA, Carling D. 1998. Identification of a Novel AMP-activated Protein Kinase ? Subunit Isoform That Is Highly Expressed in Skeletal Muscle. J. Biol. Chem.. 273(20):12443-12450.
Viollet B, Andreelli F, Jørgensen SB, Perrin C, Geloen A, Flamez D, Mu J, Lenzner C, Baud O, Bennoun M, et al. 2003. The AMP-activated protein kinase ?2 catalytic subunit controls whole-body insulin sensitivity. J. Clin. Invest.. 111(1):91-98.
Yamada E, Lee TA, Pessin JE, Bastie CC. 2010. Targeted therapies of the LKB1/AMPK pathway for the treatment of insulin resistance. Future Medicinal Chemistry. 2(12):1785-1796.
Zhou G, Myers R, Li Y, Chen Y, Shen X, Fenyk-Melody J, Wu M, Ventre J, Doebber T, Fujii N, et al. 2001. Role of AMP-activated protein kinase in mechanism of metformin action. J. Clin. Invest.. 108(8):1167-1174.

Social Media

LinkedIn icon
Twitter icon
Facebook Icon
Instagram Icon


Research. Development. Production.

We are a leading supplier to the global Life Science industry with solutions and services for research, biotechnology development and production, and pharmaceutical drug therapy development and production.

© 2021 Merck KGaA, Darmstadt, Germany and/or its affiliates. All Rights Reserved.

Reproduction of any materials from the site is strictly forbidden without permission.