Dephosphorylation is the removal of a phosphate (PO43-) group from an organic compound by hydrolysis. It is a reversible post-translational modification that is coupled to the addition of phosphate groups, or phosphorylation. A highly regulated process, dephosphorylation activates and deactivates enzymes by cleaving phosphoric esters and anhydrides. A notable occurrence of dephosphorylation is the conversion of ATP to ADP and inorganic phosphate.
Dephosphorylation employs a type of hydrolytic enzyme, or hydrolase, which cleave ester bonds. The prominent hydrolase subclass used in dephosphorylation is phosphatase. Phosphatase removes phosphate groups by hydrolysing phosphoric acid monoesters into a phosphate ion and a molecule with a free hydroxyl (-OH) group.
The reversible phosphorylation-dephosphorylation reaction occurs in every physiological process, making proper function of protein phosphases necessary for organism viability. Because protein dephosphorylation is a key process involved in cell signalling, protein phosphatases are implicated in conditions such as cardiac disease, diabetes, and Alzheimer's disease.
The discovery of dephosphorylation came from a series of experiments examining the enzyme phosphorylase isolated from rabbit skeletal muscle. In 1955, Edwin Krebs and Edmond Fischer used radiolabeled ATP to determine that phosphate is added to the serine residue of phosphorylase to convert it from its b to a form via phosphorylation. Subsequently, Krebs and Fischer showed that this phosphorylation is part of a kinase cascade. Finally, after purifying the phosphorylated form of the enzyme, phosphorylase a, from rabbit liver, ion exchange chromatography was used to identify phosphoprotein phosphatase I and II.
Since the discovery of these dephosphorylating proteins, the reversible nature of phosphorylation and dephosphorylation has been associated with a broad range of functional proteins, primarily enzymatic, but also including nonenzymatic proteins. Edwin Krebs and Edmond Fischer won the 1992 Nobel Prize in Physiology or Medicine for the discovery of reversible protein phosphorylation.
Phosphorylation and dephosphorylation of hydroxyl groups belonging to neutral but polar amino acids such as serine, threonine, and tyrosine within specific target proteins is a fundamental part of the regulation of every physiologic process. Phosphorylation involves the covalent modification of the hydroxyl with a phosphate group through the nucleophilic attack of the alpha phosphate in ATP by the oxygen in the hydroxyl. Dephosphorylation involves removal of the phosphate group through a hydration reaction by addition of a molecule of water and release of the original phosphate group, regenerating the hydroxyl. Both processes are reversible and either mechanism can be used to activate or deactivate a protein. Phosphorylation of a protein produces many biochemical effects, such as changing its conformation to alter its binding to a specific ligand to increase or reduce its activity. Phosphorylation and dephosphorylation can be used on all types of substrates, such as structural proteins, enzymes, membrane channels, signaling molecules, and other kinases and phosphatases. The sum of these processes is referred to as phosphoregulation. The deregulation of phosphorylation can lead to disease.
During the synthesis of proteins, polypeptide chains, which are created by ribosomes translating mRNA, must be processed before assuming a mature conformation. The dephosphorylation of proteins is a mechanism for modifying behavior of a protein, often by activating or inactivating an enzyme. Components of the protein synthetic apparatus also undergo phosphorylation and dephosphorylation and thus regulate the rates of protein synthesis.
As part of postranslational modifications, phosphate groups may be removed from serine, threonine, or tyrosine. As such, pathways of intracellular signal transduction depend on sequential phosphorylation and dephosphorylation of a wide variety of proteins.
ATP4- + H2O --> ADP3- + HPO42- + H+
Adenosine triphosphate, or ATP, acts as a free energy "currency" in all living organisms. In a spontaneous dephosphorylation reaction 30.5 kJ/mol is released, which is harnessed to drive cellular reactions. Overall, nonspontaneous reactions coupled to the dephosphorylation of ATP are spontaneous, due to the negative free energy change of the coupled reaction. This is important in driving oxidative phosphorylation. ATP is dephosphorylated to ADP and inorganic phosphate.
On the cellular level, the dephosphorylation of ATPases determines the flow of ions into and out of the cell. Proton pump inhibitors are a class of drug that acts directly on ATPases of the gastrointestinal tract.
Dephosphorylation in other reactions
Other molecules besides ATP undergo dephosphorylation as part of other biological systems. Different compounds produce different free energy changes as a result of dephosphorylation.
|Molecule||Change in Free Energy|
|Acetyl phosphate||47.3 kJ/mol|
|Phosphoenolpyruvate (PEP)||-61.9 kJ/mo|
Importance of Dephosphorylation in Photosystem II
The first protein complex of the photosynthesis component light-dependent reactions is referred to as photosystem II. The complex utilizes an enzyme to capture photons of light, providing the greater photosynthesis process with all of the electrons needed to produce ATP. Photosystem II is particularly temperature sensitive, and desphosphorylation has been implicated as a driver of plasticity in responding to varied temperature. Accelerated protein dephosphorylation in photosynthetic thylakoid membranes occurs at elevated temperatures, directly impacting the desphosphorylation of key proteins within the photosystem II complex.
Role of dephosphorylation in disease
Excessive dephosphorylation of the membrane ATPases and proton pumps in the gastrointestinal tract leads to higher secretory rates of caustic peptic acids. These result in heartburn and esophagitis. In combination with Helicobacter pylori infection, peptic ulcer disease is caused by the elevated pH dephosphorylation elicits.
The microtubule-associated protein tau is abnormally hyperphosphorylated when isolated from the brain of patients who suffer from Alzheimer's disease. This is due to the dysfunction of dephosphorylation mechanisms at specific amino acids on the tau protein. Tau dephosphorylation is catalysed by protein phosphatase-2A and phosphatase-2B. Deficiency or modification of one or both proteins may be involved in abnormal phosphorylation of tau in Alzheimer's disease
Dephosphorylation has also been linked to cardiac disease, particularly the alteration of actin-myosin interactions that are key for providing the underlying force of a heartbeat. Desphosphorylatoin is a key part of the myosin cycling kinetics that directly control the actin-myosin interactions. When the dephosphorylaton process is interrupted, calcium dependent cardiac contraction is impaired or fully disabled.
Research has also suggested that modifications to dephosphorylation impact physiological processes implicated in Diabetes mellitus. The kinetics of dephosphorylation of insulin receptor substrate-1/2, Akt, and ERK1/2, phosphoproteins are shown to be involved in insulin receptor signaling, and in vitro models demonstrate that changes to dephosphorylation kinetics impact upstram and downstream insulin stimulation.
Inhibition of proton pumps significantly decreases the acidity of the gastrointestinal tract, reducing the symptoms of acid-related diseases. The resulting change in pH decreases survival of the bacteria H.pylori, a major cause of peptic ulcer disease. Once the proton pump inhibitor eradicates this bacteria within the gut, reversing erosive reflux. Treating heart disease has improved with the use of drugs that inhibit AMPK via dephosphorylation. In the treatment of diabetes, sulfonylurea drugs are able to stimulate dephosphorylation of the glucose transporter GLUT4, decreasing insulin resistance and increasing and glucose utilization.
Dephosphorylation can play a key role in molecular biology, particularly cloning using restriction enzymes. The cut ends of a vector may re-ligate during a ligation step due to phosphorylation. By using a desphosphorylating phosphatase, re-ligation can be avoided. These alkaline phosphatases are often sourced naturally, most commonly from calf intestine, and are abbreviated as CIP.
- FISCHER, EH; KREBS, EG (1955 Sep). "Conversion of phosphorylase b to phosphorylase a in muscle extracts.". The Journal of Biological Chemistry 216 (1): 121–32. PMID 13252012.
- Khandelwal, RL; Vandenheede, JR; Krebs, EG (1976 Aug 25). "Purification, properties, and substrate specificities of phosphoprotein phosphatase(s) from rabbit liver.". The Journal of Biological Chemistry 251 (16): 4850–8. PMID 8449.
- Krebs EG, Beavo JA (1979). "Phosphorylation-dephosphorylation of enzymes". Annu. Rev. Biochem. 48: 923–59. doi:10.1146/annurev.bi.48.070179.004423. PMID 38740.
- Raju TN (June 2000). "The Nobel chronicles. 1992: Edmond H Fischer (b 1920) and Edwin G Krebs (b 1918)". Lancet 355 (9219): 2004. doi:10.1016/S0140-6736(05)72951-2. PMID 10859071.
- PDB 1d5r; Lee JO, Yang H, Georgescu MM, Di Cristofano A, Maehama T, Shi Y, Dixon JE, Pandolfi P, Pavletich NP (October 1999). "Crystal structure of the PTEN tumor suppressor: implications for its phosphoinositide phosphatase activity and membrane association". Cell 99 (3): 323–34. doi:10.1016/S0092-8674(00)81663-3. PMID 10555148.
- Beltrao P, Trinidad JC, Fiedler D, et al. (June 2009). "Evolution of phosphoregulation: comparison of phosphorylation patterns across yeast species". PLoS Biol. 7 (6): e1000134. doi:10.1371/journal.pbio.1000134. PMC 2691599. PMID 19547744.
- Bononi A, Agnoletto C, De Marchi E, et al. (2011). "Protein kinases and phosphatases in the control of cell fate". Enzyme Res 2011: 329098. doi:10.4061/2011/329098. PMC 3166778. PMID 21904669.
- Celis JE, Madsen P, Ryazanov AG (June 1990). "Increased phosphorylation of elongation factor 2 during mitosis in transformed human amnion cells correlates with a decreased rate of protein synthesis". Proc. Natl. Acad. Sci. U.S.A. 87 (11): 4231–5. PMC 54082. PMID 2349232.
- Casiday, Rachel. "Energy for the Body: Oxidative Phosphorylation". Retrieved 5 April 2013.
- Casiday, Rachel. "Oxidation-Reduction Reactions Experiment". Energy for the Body: Oxidative Phosphorylation. Department of Chemistry, Washington University. Retrieved 24 April 2013.
- Yamauchi, Yasuo (29). "Plants switch photosystem at high temperature to protect photosystem II". Plant Biology.
- Rokka, A; Aro, EM; Herrmann, RG; Andersson, B; Vener, AV (2000 Aug). "Dephosphorylation of photosystem II reaction center proteins in plant photosynthetic membranes as an immediate response to abrupt elevation of temperature.". Plant physiology 123 (4): 1525–36. PMID 10938368.
- Robinson, M (2005 Jun). "Proton pump inhibitors: update on their role in acid-related gastrointestinal diseases.". International journal of clinical practice 59 (6): 709–15. PMID 15924600.
- Gong CX, Grundke-Iqbal I, Iqbal K (August 1994). "Dephosphorylation of Alzheimer's disease abnormally phosphorylated tau by protein phosphatase-2A". Neuroscience 61 (4): 765–72. PMID 7838376.
- Sheikh F, Ouyang K, Campbell SG, et al. (April 2012). "Mouse and computational models link Mlc2v dephosphorylation to altered myosin kinetics in early cardiac disease". J. Clin. Invest. 122 (4): 1209–21. doi:10.1172/JCI61134. PMC 3314469. PMID 22426213.
- Zhande R, Zhang W, Zheng Y, et al. (December 2006). "Dephosphorylation by default, a potential mechanism for regulation of insulin receptor substrate-1/2, Akt, and ERK1/2". J. Biol. Chem. 281 (51): 39071–80. doi:10.1074/jbc.M605251200. PMID 17068339.
- Hutchinson, DS; Summers, RJ; Bengtsson, T (2008 Sep). "Regulation of AMP-activated protein kinase activity by G-protein coupled receptors: potential utility in treatment of diabetes and heart disease.". Pharmacology & therapeutics 119 (3): 291–310. PMID 18606183.
- Müller, G; Wied, S (1993 Dec). "The sulfonylurea drug, glimepiride, stimulates glucose transport, glucose transporter translocation, and dephosphorylation in insulin-resistant rat adipocytes in vitro.". Diabetes 42 (12): 1852–67. PMID 8243832.
- Sambrook, J; Fritsch, E.F., Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual (2nd ed.). Cold Spring Harbor Laboratory Press.
- Makovets S, Blackburn EH (November 2009). "DNA damage signalling prevents deleterious telomere addition at DNA breaks". Nat. Cell Biol. 11 (11): 1383–6. doi:10.1038/ncb1985. PMC 2806817. PMID 19838171.