Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound   Target Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound

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Query: EC:3.1.4.1 (phosphodiesterase)
18,767 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Two different methods were used to study directly alpha-thrombin modulation of polyphosphoinositide breakdown in membranes prepared from Chinese hamster lung (CHL) fibroblasts. In the first one we labelled the lipid pool by incubating the intact cells with myo-[3H]inositol prior to membrane isolation; in the other we used exogenous [3H]PIP2 with phosphatidylethanolamine (1:10) added as liposomes to freshly isolated membranes. A Ca2+-dependent PIP2 and PIP phospholipase C activity was characterized by measuring the rate of formation of inositol tris- and bisphosphate. Basal phospholipase C activity was stimulated up to 3-fold by GTP or GTP-gamma-S. Of the two mitogens, alpha-thrombin and EGF, known to stimulate DNA synthesis in Chinese hamster fibroblasts, only alpha-thrombin is a potent activator of PIP2 breakdown in intact cells. Consistent with this observation, alpha-thrombin but not EGF potentiated GTP-gamma-S-dependent phospholipase C activity in membrane preparations. These results strongly support the hypothesis that a GTP-binding protein couples alpha-thrombin receptor to PIP2 hydrolysis. Because both methods used to assay phospholipase C gave identical results, we conclude that the coupling is at the level of PIP2-phosphodiesterase activity.
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PMID:Evidence for a GTP-binding protein coupling thrombin receptor to PIP2-phospholipase C in membranes of hamster fibroblasts. 302 38

Transducin is a GTP-binding protein which mediates the light activation signal from photolyzed rhodopsin to cGMP phosphodiesterase and is pivotal in the visual excitation process. Biochemical studies suggest that the T alpha subunit of transducin is composed of three functional domains, one for rhodopsin/T beta gamma interaction, another for guanine nucleotide binding, and a third for the activation of phosphodiesterase. The integration of the primary sequence of T alpha along with secondary structure, hydropathy and folding topology predictions, and a comparison with homologous proteins have led to the construction of a three-dimensional model of the T alpha subunit. A molecular mechanism which underlies the coupling action of T alpha is suggested on the basis of this model.
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PMID:A structural model for the alpha-subunit of transducin. Implications of its role as a molecular switch in the visual signal transduction mechanism. 303 11

The hydrolysis of [3H]phosphatidylinositol (PI) and [3H]phosphatidylinositol-4,5-bisphosphate (PIP2) by cytosolic inositide phosphodiesterase (phospholipase C) from Ehrlich ascites tumour cells was determined. Cytosolic fractions were prepared from tumour cells that had been cultivated for two days at low serum level (2%) in the presence of 1-oleoyl-2-acetyl-sn-glycerol (OAG). Cytosols from unstimulated cells (2% serum without OAG) were used for comparison. Phospholipase C acting on PI and PIP2 was significantly inhibited in the cytosol of OAG-stimulated cells. The suppressed enzyme was activated by Ca2+ and also by the guanine nucleotide GTP in a concentration-dependent manner independently of calcium ions. In the presence of Ca2+, GTP exerted a synergistic stimulatory effect. In contrast, GTP and GTP gamma S showed no effect on the phospholipase C activity of unstimulated cells. It is suggested that the suppressed PI- and PIP2-specific enzyme activity can be modulated by its susceptibility to Ca2+ ions and GTP probably via the GTP-binding protein.
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PMID:Guanine nucleotides activate cytosolic phospholipase C of ascites tumour cells stimulated by 1-oleoyl-2-acetyl-sn-glycerol. 325 Sep 42

Light exposure of rhodopsin in rod outer segment (ROS) membranes activates several cyclic GMP phosphodiesterase (PDE) molecules via a GTP-binding protein (G protein). Both PDE and G protein are surface-associated (peripheral) enzymes, which may be extracted from ROS by hypotonic media, individually purified, and recombined in isotonic media with purified rhodopsin-phospholipid vesicles to yield membranes of low dark and high light phosphodiesterase activity. In isotonic media, the PDE strongly associates with phospholipid membranes as well as with ROS and rhodopsin-phospholipid membranes. Because only membrane-associated PDE is readily light activated, the PDE activity saturates when the available binding sites are occupied. At a constant G-protein concentration, the PDE activity observed at saturation is 4 times greater for unilamellar rhodopsin-phospholipid vesicles with a lipid to rhodopsin ratio of 460 than for those with a ratio of 120. Thus, PDE association with membrane in isotonic media is dependent on the phospholipid content rather than the rhodopsin content. Several G proteins per PDE are necessary to maximize the PDE activity of reconstituted membranes; therefore, a weak association between activated G protein and PDE is indicated. Both peripheral enzymes readily transfer between membrane surfaces. Rhodopsin-phospholipid vesicles devoid of enzyme activity were exposed to a light flash and then mixed in the dark in isotonic media with unilluminated ROS membranes which contained PDE and G protein. PDE activity was observed within 2 s after mixing. Subsequent separation and evaluation of the denser ROS membranes and the less dense vesicles demonstrated that both PDE and G protein were associated with the vesicles as well as the ROS membranes.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Rod outer segment phosphodiesterase binding and activation in reconstituted membranes. 609 33

Bovine serum albumin inhibits the light activation of bovine rod disc membrane (RDM) cyclic GMP phosphodiesterase. The KI for inhibition is 32 microM at pH 8 and 37 degrees C. Trypsin-activated phosphodiesterase was not inhibited under these conditions, suggesting that albumin does not alter substrate access to the enzyme. Light titration curves of phosphodiesterase activity were vertically displaced downwards by albumin. The lack of displacement along the bleach axis indicated no loss in relative light sensitivity, but rather loss of a constant fraction of the normal activity for each bleach level. Thus, activated rhodopsin appeared to be functional in the presence of albumin. However, the metarhodopsin II yield with less than 10% bleached was reduced in the presence of albumin. This effect was quantitatively explained by albumin elution of GTP-binding protein from the RDM. Similarly, the reduction in light-induced phosphodiesterase activity quantitatively matched GTP-binding protein elution by albumin. beta-Lactoglobulin, which, like albumin, is known to bind hydrophobic molecules, also inhibits phosphodiesterase activation. In contrast, ovalbumin, which has little hydrophobic binding affinity, had little or no inhibitory effect on phosphodiesterase light activation. We conclude that albumin and other molecules capable of hydrophobic interactions inhibit light activation of RDM-phosphodiesterase by selectively eluting GTP-binding protein from the membrane into the surrounding medium where it is unable to efficiently gain access to activated rhodopsin.
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PMID:Albumin inhibits light activation of cGMP phosphodiesterase on rod disc membranes. 609 63

We find prompt, high stoichiometry phosphorylation of rhodopsin in response to low fractional rhodopsin bleaching in bovine rod outer segments (ROS). For example, 4 +/- 1 phosphates are incorporated per bleached rhodopsin (Rho*) in 30 sec and 6 +/- 2 phosphates are incorporated in 75 sec in response to bleaching 1% of the rhodopsin in the presence of 1 mM [gamma-32P]ATP and 0.1 mM nonradioactive GTP. Omission of GTP leads to ca 70% inhibition of rhodopsin phosphorylation, presumably due to the GTP-binding protein blocking access of rhodopsin kinase to rhodopsin. Light induced phosphodiesterase (PDE) activation is rapidly quenched in the presence of ATP as first reported by by Liebman and Pugh [Nature 287, 734-736 (1980)]. The kinetics of rhodopsin phosphorylation vary with conditions and from preparation to preparation, however, they are always at least as fast as the ATP dependent quenching of PDE activation. The maximum extent of rhodopsin phosphorylation was limited by specific proteolytic trimming of the carboxyl-terminal phosphorylation sites in washed ROS membranes "stripped" of extrinsic proteins. Membrane preparations with 6,4,2, or 1 phosphate(s) incorporated/Rho* (after a 75 sec post bleach incubation) were produced by treatment with: no protease, carboxypeptidase Y (C), trypsin (T), or both T and C (TC), respectively, followed by reassociation with extrinsic membrane proteins and phosphorylation. Low fractional bleaching was required for maximum phosphorylation/Rho* in membranes which were stripped and reassociated with extrinsic proteins and in isolated ROS. Removal of C-terminal rhodopsin phosphorylation sites has little or no effect on light activation of PDE in the absence of ATP. However, in the presence of ATP the extent of the removal of C-terminal rhodopsin residues has large effects on the light activation and the shut-off of PDE. The single phosphate/Rho* that was added to TC digested membranes reduced the lifetime of Rho* but apparently was not incorporated rapidly enough under our conditions to inhibit the Vmax of PDE. The two phosphates/Rho* which were incorporated after T digestion cause a large decrease in the lifetime of Rho* as well as a decrease in the Vmax of PDE (at low bleaching levels). The four phosphates/Rho* that were added after C digestion further reduce the lifetime of Rho* and the Vmax of PDE. The 6 phosphates/Rho* which were incorporated into the unproteolyzed membranes have little additional effect on Rho* lifetime compared to 4 phosphates/Rho*. However, increasing the phosphorylation observed from 4 to 6 phosphates greatly inhibits the Vmax of PDE at intermediate bleaching levels.(ABSTRACT TRUNCATED AT 400 WORDS)
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PMID:Phosphorylation at sites near rhodopsin's carboxyl-terminus regulates light initiated cGMP hydrolysis. 609 32

The binding of cyclic GMP phosphodiesterase (PDE) to bovine rod outer segment membranes has been measured under various conditions of ionic strength, light and darkness and with and without added GTP. Comparison of the effects of magnesium, calcium and sodium ions shows that it is ionic strength rather than the nature of the ion that determines the binding, and that Ca2+ has no special properties in this respect. The level of light-induced activity of the bound PDE has been measured under the different conditions, and this shows that a relatively constant proportion (1-5%) of the bound PDE is in an active site irrespective of how the membranes have been washed. This means that sufficient GTP-binding protein (GBP) is also bound to the membranes to maintain a constant proportion of active PDE. The washed membranes are capable of activating more PDE molecules than those already bound, and even bleached membranes washed twice with GTP-containing, low-ionic strength buffers could activate considerable numbers of added PDE molecules. These experiments suggest that under the ionic strength conditions of the intact cell effectively all of the PDE is membrane bound, and that exposure to light or changes in the Ca2+ concentration are unlikely to cause significant changes in the amount of PDE bound, or to the level of its activity.
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PMID:The effects of ionic concentration and light on the binding of enzymes to rod outer segment membranes. 609 33

We describe a reconstitution of light-activated vertebrate photoreceptor GTPase and a purification of the GTP-binding protein (G protein), which is a component of the GTPase and modulates the light-activated phosphodiesterase (PDE) enzyme system. Rod outer segments (ROS) of bull frogs were treated with ethylenediaminetetraacetic acid (EDTA), and the GTPase and PDE fractions were solubilized (EDTA supernatant). When the EDTA supernatant and EDTA-treated membrane fraction (EDTA-washed membranes) were recombined, light-dependent GTPase activity appeared. In the reconstituted system, the Km for GTP as substrate was 0.5 microM; the optimum pH was 7.5-8.0. The isoelectric point of GTPase in EDTA supernatant was 4.8. G protein was purified 400-fold from ROS, and the molecular weight of G protein was determined to be 40 000 by polyacrylamide gel electrophoresis. The amount of G protein in ROS was calculated as at least 1 molecule per 400 rhodopsin molecules. By recombining (in the presence or absence of GTP) purified G protein, PDE, H fraction (an additional component of GTPase), and illuminated or unilluminated EDTA-washed membranes (as a source of rhodopsin), we showed that illuminated rhodopsin, G protein, PDE, and GTP are the minimum requirements for light-dependent PDE activity. We discuss the significance of these findings in the regulation of the light-activated GTPase and PDE activities, especially with regard to the mechanism of activation.
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PMID:Purification and characteristics of photoreceptor light-activated guanosinetriphosphatase. 611 10

Prolonged exposure to beta-adrenergic agonists of pigeon erythrocytes causes a reversible loss (70%) of catecholamine-stimulated adenylate cyclase activity without reduction in the number of beta-adrenergic receptors. In addition a less pronounced decrease in non-stimulated and NaF-stimulated adenylate cyclase activity (15-22%) is observed, appearing at different agonist concentrations and at a different rate. Dibutyryladenosine 3',5'-phosphate and the phosphodiesterase inhibitor methylisobutylxanthine partially mimick the action of the beta-adrenergic agonist, thus pointing to a possible role of adenosine 3',5'-phosphate in establishing desensitization. When adenylate cyclase from desensitized cells is stimulated with 5'-guanylyl-imidodiphosphate in the presence or absence of catecholamines the lag period preceding the attainment of maximal activity is extended. Likewise the rate of reversal by GTP or GTP of persistent activation of adenylate cyclase is slowed down. This is therefore interpreted to mean that the loss in hormonal stimulation on treatment of pigeon red blood cells with beta-adrenergic agonists is due to a delayed exchange of GDP against GTP on the regulatory GTP-binding protein. Furthermore, we conclude that events causing the refractory state in avian erythrocytes should occur at a site distal to the beta-adrenergic receptor.
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PMID:Functional desensitisation of beta-adrenergic receptors of avian erythrocytes by catecholamines and adenosine 3',5'-phosphate. 616 40

A specific protein associated with rod-outer-segment disc membranes binds GTP only in the presence of bleached rhodopsin. Once formed the protein-GTP complex becomes a soluble activator of cGMP phosphodiesterase. It is shown that this activator complex can be completely separated from rhodopsin and retain its ability to activate phosphodiesterase when added to a pool of totally dark (unilluminated) disc membranes. The photoreactive GTP analogue p3-(4-azidoanilido)-5' GTP (AAGTP) is shown to be a more effective substrate than GTP, Gpp(NH)p or 8-azido GTP. [8, 5' 3H] AAGTP was used to specifically covalently label the GTP-binding protein. The protein labeled exhibits a mass of 40,000 daltons when analyzed by SDS-PAGE.
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PMID:A GTP-protein activator of phosphodiesterase which forms in response to bleached rhodopsin. 627 4


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