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Biochemical Journal logoLink to Biochemical Journal
. 1999 Mar 15;338(Pt 3):717–722.

AMP-activated protein kinase: an ultrasensitive system for monitoring cellular energy charge.

D G Hardie 1, I P Salt 1, S A Hawley 1, S P Davies 1
PMCID: PMC1220108  PMID: 10051444

Abstract

The AMP-activated protein kinase cascade is activated by elevation of AMP and depression of ATP when cellular energy charge is compromised, leading to inhibition of anabolic pathways and activation of catabolic pathways. Here we show that the system responds in intact cells in an ultrasensitive manner over a critical range of nucleotide concentrations, in that only a 6-fold increase in activating nucleotide is required in order for the maximal activity of the kinase to progress from 10% to 90%, equivalent to a co-operative system with a Hill coefficient (h) of 2.5. Modelling suggests that this sensitivity arises from two features of the system: (i) AMP acts at multiple steps in the cascade (multistep sensitivity); and (ii) the upstream kinase is initially saturated with the downstream kinase (zero-order ultrasensitivity).

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Selected References

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  1. Blumer K. J., Johnson G. L. Diversity in function and regulation of MAP kinase pathways. Trends Biochem Sci. 1994 Jun;19(6):236–240. doi: 10.1016/0968-0004(94)90147-3. [DOI] [PubMed] [Google Scholar]
  2. Chock P. B., Stadtman E. R. Superiority of interconvertible enzyme cascades in metabolite regulation: analysis of multicyclic systems. Proc Natl Acad Sci U S A. 1977 Jul;74(7):2766–2770. doi: 10.1073/pnas.74.7.2766. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Corton J. M., Gillespie J. G., Hardie D. G. Role of the AMP-activated protein kinase in the cellular stress response. Curr Biol. 1994 Apr 1;4(4):315–324. doi: 10.1016/s0960-9822(00)00070-1. [DOI] [PubMed] [Google Scholar]
  4. Corton J. M., Gillespie J. G., Hawley S. A., Hardie D. G. 5-aminoimidazole-4-carboxamide ribonucleoside. A specific method for activating AMP-activated protein kinase in intact cells? Eur J Biochem. 1995 Apr 15;229(2):558–565. doi: 10.1111/j.1432-1033.1995.tb20498.x. [DOI] [PubMed] [Google Scholar]
  5. Dale S., Wilson W. A., Edelman A. M., Hardie D. G. Similar substrate recognition motifs for mammalian AMP-activated protein kinase, higher plant HMG-CoA reductase kinase-A, yeast SNF1, and mammalian calmodulin-dependent protein kinase I. FEBS Lett. 1995 Mar 20;361(2-3):191–195. doi: 10.1016/0014-5793(95)00172-6. [DOI] [PubMed] [Google Scholar]
  6. Davies S. P., Carling D., Hardie D. G. Tissue distribution of the AMP-activated protein kinase, and lack of activation by cyclic-AMP-dependent protein kinase, studied using a specific and sensitive peptide assay. Eur J Biochem. 1989 Dec 8;186(1-2):123–128. doi: 10.1111/j.1432-1033.1989.tb15185.x. [DOI] [PubMed] [Google Scholar]
  7. Davies S. P., Hawley S. A., Woods A., Carling D., Haystead T. A., Hardie D. G. Purification of the AMP-activated protein kinase on ATP-gamma-sepharose and analysis of its subunit structure. Eur J Biochem. 1994 Jul 15;223(2):351–357. doi: 10.1111/j.1432-1033.1994.tb19001.x. [DOI] [PubMed] [Google Scholar]
  8. Davies S. P., Helps N. R., Cohen P. T., Hardie D. G. 5'-AMP inhibits dephosphorylation, as well as promoting phosphorylation, of the AMP-activated protein kinase. Studies using bacterially expressed human protein phosphatase-2C alpha and native bovine protein phosphatase-2AC. FEBS Lett. 1995 Dec 27;377(3):421–425. doi: 10.1016/0014-5793(95)01368-7. [DOI] [PubMed] [Google Scholar]
  9. Ferrell J. E., Jr, Machleder E. M. The biochemical basis of an all-or-none cell fate switch in Xenopus oocytes. Science. 1998 May 8;280(5365):895–898. doi: 10.1126/science.280.5365.895. [DOI] [PubMed] [Google Scholar]
  10. Ferrell J. E., Jr Tripping the switch fantastic: how a protein kinase cascade can convert graded inputs into switch-like outputs. Trends Biochem Sci. 1996 Dec;21(12):460–466. doi: 10.1016/s0968-0004(96)20026-x. [DOI] [PubMed] [Google Scholar]
  11. Goldbeter A., Koshland D. E., Jr An amplified sensitivity arising from covalent modification in biological systems. Proc Natl Acad Sci U S A. 1981 Nov;78(11):6840–6844. doi: 10.1073/pnas.78.11.6840. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hardie D. G., Carling D., Carlson M. The AMP-activated/SNF1 protein kinase subfamily: metabolic sensors of the eukaryotic cell? Annu Rev Biochem. 1998;67:821–855. doi: 10.1146/annurev.biochem.67.1.821. [DOI] [PubMed] [Google Scholar]
  13. Hardie D. G., Carling D. The AMP-activated protein kinase--fuel gauge of the mammalian cell? Eur J Biochem. 1997 Jun 1;246(2):259–273. doi: 10.1111/j.1432-1033.1997.00259.x. [DOI] [PubMed] [Google Scholar]
  14. Hawley S. A., Davison M., Woods A., Davies S. P., Beri R. K., Carling D., Hardie D. G. Characterization of the AMP-activated protein kinase kinase from rat liver and identification of threonine 172 as the major site at which it phosphorylates AMP-activated protein kinase. J Biol Chem. 1996 Nov 1;271(44):27879–27887. doi: 10.1074/jbc.271.44.27879. [DOI] [PubMed] [Google Scholar]
  15. Hawley S. A., Selbert M. A., Goldstein E. G., Edelman A. M., Carling D., Hardie D. G. 5'-AMP activates the AMP-activated protein kinase cascade, and Ca2+/calmodulin activates the calmodulin-dependent protein kinase I cascade, via three independent mechanisms. J Biol Chem. 1995 Nov 10;270(45):27186–27191. doi: 10.1074/jbc.270.45.27186. [DOI] [PubMed] [Google Scholar]
  16. Hayashi T., Hirshman M. F., Kurth E. J., Winder W. W., Goodyear L. J. Evidence for 5' AMP-activated protein kinase mediation of the effect of muscle contraction on glucose transport. Diabetes. 1998 Aug;47(8):1369–1373. doi: 10.2337/diab.47.8.1369. [DOI] [PubMed] [Google Scholar]
  17. Henin N., Vincent M. F., Gruber H. E., Van den Berghe G. Inhibition of fatty acid and cholesterol synthesis by stimulation of AMP-activated protein kinase. FASEB J. 1995 Apr;9(7):541–546. doi: 10.1096/fasebj.9.7.7737463. [DOI] [PubMed] [Google Scholar]
  18. Henin N., Vincent M. F., Van den Berghe G. Stimulation of rat liver AMP-activated protein kinase by AMP analogues. Biochim Biophys Acta. 1996 Jun 4;1290(2):197–203. doi: 10.1016/0304-4165(96)00021-9. [DOI] [PubMed] [Google Scholar]
  19. Huang C. Y., Ferrell J. E., Jr Ultrasensitivity in the mitogen-activated protein kinase cascade. Proc Natl Acad Sci U S A. 1996 Sep 17;93(19):10078–10083. doi: 10.1073/pnas.93.19.10078. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Hutber C. A., Hardie D. G., Winder W. W. Electrical stimulation inactivates muscle acetyl-CoA carboxylase and increases AMP-activated protein kinase. Am J Physiol. 1997 Feb;272(2 Pt 1):E262–E266. doi: 10.1152/ajpendo.1997.272.2.E262. [DOI] [PubMed] [Google Scholar]
  21. Kholodenko B. N., Hoek J. B., Westerhoff H. V., Brown G. C. Quantification of information transfer via cellular signal transduction pathways. FEBS Lett. 1997 Sep 8;414(2):430–434. doi: 10.1016/s0014-5793(97)01018-1. [DOI] [PubMed] [Google Scholar]
  22. Koshland D. E., Jr, Goldbeter A., Stock J. B. Amplification and adaptation in regulatory and sensory systems. Science. 1982 Jul 16;217(4556):220–225. doi: 10.1126/science.7089556. [DOI] [PubMed] [Google Scholar]
  23. Kudo N., Barr A. J., Barr R. L., Desai S., Lopaschuk G. D. High rates of fatty acid oxidation during reperfusion of ischemic hearts are associated with a decrease in malonyl-CoA levels due to an increase in 5'-AMP-activated protein kinase inhibition of acetyl-CoA carboxylase. J Biol Chem. 1995 Jul 21;270(29):17513–17520. doi: 10.1074/jbc.270.29.17513. [DOI] [PubMed] [Google Scholar]
  24. Meinke M. H., Edstrom R. D. Muscle glycogenolysis. Regulation of the cyclic interconversion of phosphorylase a and phosphorylase b. J Biol Chem. 1991 Feb 5;266(4):2259–2266. [PubMed] [Google Scholar]
  25. Merrill G. F., Kurth E. J., Hardie D. G., Winder W. W. AICA riboside increases AMP-activated protein kinase, fatty acid oxidation, and glucose uptake in rat muscle. Am J Physiol. 1997 Dec;273(6 Pt 1):E1107–E1112. doi: 10.1152/ajpendo.1997.273.6.E1107. [DOI] [PubMed] [Google Scholar]
  26. Ponticos M., Lu Q. L., Morgan J. E., Hardie D. G., Partridge T. A., Carling D. Dual regulation of the AMP-activated protein kinase provides a novel mechanism for the control of creatine kinase in skeletal muscle. EMBO J. 1998 Mar 16;17(6):1688–1699. doi: 10.1093/emboj/17.6.1688. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Rasmussen B. B., Winder W. W. Effect of exercise intensity on skeletal muscle malonyl-CoA and acetyl-CoA carboxylase. J Appl Physiol (1985) 1997 Oct;83(4):1104–1109. doi: 10.1152/jappl.1997.83.4.1104. [DOI] [PubMed] [Google Scholar]
  28. Salt I. P., Johnson G., Ashcroft S. J., Hardie D. G. AMP-activated protein kinase is activated by low glucose in cell lines derived from pancreatic beta cells, and may regulate insulin release. Biochem J. 1998 Nov 1;335(Pt 3):533–539. doi: 10.1042/bj3350533. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Salt I., Celler J. W., Hawley S. A., Prescott A., Woods A., Carling D., Hardie D. G. AMP-activated protein kinase: greater AMP dependence, and preferential nuclear localization, of complexes containing the alpha2 isoform. Biochem J. 1998 Aug 15;334(Pt 1):177–187. doi: 10.1042/bj3340177. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Stapleton D., Mitchelhill K. I., Gao G., Widmer J., Michell B. J., Teh T., House C. M., Fernandez C. S., Cox T., Witters L. A. Mammalian AMP-activated protein kinase subfamily. J Biol Chem. 1996 Jan 12;271(2):611–614. doi: 10.1074/jbc.271.2.611. [DOI] [PubMed] [Google Scholar]
  31. Vavvas D., Apazidis A., Saha A. K., Gamble J., Patel A., Kemp B. E., Witters L. A., Ruderman N. B. Contraction-induced changes in acetyl-CoA carboxylase and 5'-AMP-activated kinase in skeletal muscle. J Biol Chem. 1997 May 16;272(20):13255–13261. doi: 10.1074/jbc.272.20.13255. [DOI] [PubMed] [Google Scholar]
  32. Velasco G., Geelen M. J., Guzmán M. Control of hepatic fatty acid oxidation by 5'-AMP-activated protein kinase involves a malonyl-CoA-dependent and a malonyl-CoA-independent mechanism. Arch Biochem Biophys. 1997 Jan 15;337(2):169–175. doi: 10.1006/abbi.1996.9784. [DOI] [PubMed] [Google Scholar]
  33. Winder W. W., Hardie D. G. Inactivation of acetyl-CoA carboxylase and activation of AMP-activated protein kinase in muscle during exercise. Am J Physiol. 1996 Feb;270(2 Pt 1):E299–E304. doi: 10.1152/ajpendo.1996.270.2.E299. [DOI] [PubMed] [Google Scholar]
  34. Woods A., Salt I., Scott J., Hardie D. G., Carling D. The alpha1 and alpha2 isoforms of the AMP-activated protein kinase have similar activities in rat liver but exhibit differences in substrate specificity in vitro. FEBS Lett. 1996 Nov 18;397(2-3):347–351. doi: 10.1016/s0014-5793(96)01209-4. [DOI] [PubMed] [Google Scholar]

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