Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:6.3.5.5 (CPS)
 1,262 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The effect of the phosphorylated protein, phosvitin, on the formation of the calcium phosphate crystal was examined in metastable calcium phosphate solution. Addition of glass ceramics caused consumption of hydrochloric acid, as a result of the dissolution of metal oxides. The activities of dissolution and nucleation were both high in the case of CPS-SiC. Phosvitin affected only the nucleation process, not the dissolution process. The decrease of phosvitin concentration after the addition of materials demonstrated adsorption of phosvitin by the material surface. The thermodynamic stability of solution after several days maintained equilibrium against tricalcium phosphate (TCP) and especially against octacalcium phosphate (OCP). From these results, it is concluded that glass ceramic implants have potential to stimulate hydroxyapatite formation, even in the presence of matrix substances.
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PMID:[Formation of calcium phosphate crystals in pseudophysiological solution by SiC Whisker reinforced glass ceramics. Effect of Phosvitin on nucleation]. 263 70

We reported previously that C-reactive protein (CRP), when complexed to a multivalent binding specificity, can bind to a subset of lymphocytes that bear the IgG Fc receptor. Recently we showed that anti-CRP plus complement depletes natural killer function. We now show the detection of CRP on the surface (S-CRP) of a small percentage of PBL and on a minor population of phagocytic mononuclear cells. S-CRP is not detectable by direct immunofluorescence, but is readily discernible by using more sensitive techniques such as biotinylated anti-CRP with fluorescent avidin or indirect immunofluorescence with monoclonal anti-CRP. S-CRP is expressed in the absence of calcium, whereas the binding of complexed CRP is calcium dependent. S-CRP does not appear to be the exclusive binding site for CRP-CPS because anti-CRP does not block the binding of complexed CRP. Both the binding site for complexed CRP and S-CRP can be capped off; however, the kinetics of capping of these two surface molecules is different. Cells binding complexed CRP are OKT11-, whereas a significant number of PBL bearing S-CRP are OKT11+. Therefore cells bearing S-CRP appear to be a separate population from those that bind complexed CRP. These studies establish the presence of S-CRP on a subpopulation of lymphocytes, define conditions required for its detection, and speak to certain of the relationships between S-CRP and the binding site of CRP-CPS complexes.
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PMID:C-reactive protein antigenicity on the surface of human lymphocytes. 635 57

Some properties of carbamoyl-phosphate synthetase (ammonia) were studied in rat-liver mitochondria made selectively permeable by pretreatment with toluene. The Michaelis constants for NH3, MgATP and HCO-3 were 0.7, 1.2 and 2 mM respectively. N-Acetylglutamate activated the enzyme with a Ka of about 0.1 mM. At saturating concentrations of substrates and effectors the enzyme was inhibited by 50% by carbamoyl phosphate at a concentration of 13 mM. Binding of N-acetylglutamate to carbamoyl-phosphate synthetase required the presence of both free Mg2+ ions and MgATP, and was inhibited by Ca2+ ions and by N-carbamoylglutamate. The known activation of carbamoyl-phosphate synthetase by free Mg2+ is due to an increased affinity of the enzyme for N-acetylglutamate. Binding of N-acetylglutamate to carbamoyl-phosphate synthetase was a slow process: at N-acetylglutamate concentrations below 0.5 mM maximal binding was not completed within 30 min. The rate of binding increased with increasing N-acetylglutamate concentrations. Dissociation of N-acetylglutamate from the enzyme was relatively fast, with a half-time of about 5 min. Under all conditions studied there was a close relationship between carbamoyl-phosphate synthetase activity and the amount of N-acetylglutamate bound to the enzyme. The data are discussed in relation to the control of carbamoyl-phosphate synthetase in the intact hepatocyte.
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PMID:Properties of carbamoyl-phosphate synthetase (ammonia) in rat-liver mitochondria made permeable with toluene. 688 64

C-reactive protein (RP) and serum amyloid P component (SAP) have been identified for the first time in rat serum and isolated by calcium-dependent affinity chromatography. Rat CRP closely resembled human CRP in its amino acid composition, in having five subunits per molecule and in its electron microscopic appearance as a pentameric annular disc. It differed, however, from all other mammalian CRP's characterised hitherto in being a glycoprotein bearing a single complex oligosaccharide on each polypeptide subunit. Furthermore one pair of tis subunits per molecule was linked by a interchain disulphide bridges whereas in other animals the subunits of both CRP and SAP are all non-covalently associated. The serum concentration of CRP in normal healthy laboratory rats and in specific pathogen-free rats was 300-600 micrograms/ml which is much greater than has been described in any other species and exceeds even maximal acute phase levels of CRP in man. Following injections of casein or croton oil, serum CRP levels rose to a maximum of about 900 micrograms/ml. Rat CRP bound to pneumococcal C-polysaccharide (CPS( but, in marked contrast to the behaviour of CRP from man, rabbit and marine teleost fish, it did not precipitate with CPS solutions, agglutinate CPS-coated sheep erythrocytes or initiate complement activation. Rat SAP, like SAP of other species, was a glycoprotein but unlike them it was composed only of a single pentameric disc not two such discs interacting face-to-face. The normal level of SAP in rat serum was 20-50 micrograms/ml, very similar to the levels seen in man, and it did not behave as an acute phase reactant in response to casein or croton-oil injections. In this respect it resembled human SAP but differed from murine SAP which is a major acute phase reactant.
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PMID:Isolation and characterization of C-reactive protein and serum amyloid P component in the rat. 705 68

The visible cobalt circular dichroism (CD) of cobalt-substituted concanavalin A (Con A) is highly sensitive to Ca2+-induced conformational changes that occur in the metal binding region. The observed ellipticity is separately resolved into discrete conformational spectra with separate extrinsic bands. The conformational forms of the metal region are further delineated on the basis of their differential spectral response to the competitive removal of metals by ethylene-diaminetetraacetic acid (EDTA). The spectral forms sensitive to the effects of EDTA, cobalt-Con A (CPS, epsilon CPS470 - 215 M-1) and calcium-cobalt-Con A (CaCPS, epsilon CaCPS470 = 141 M-1), exhibit both unique extinctions and band shapes in the 400-500-nm region, as does the fully metalized EDTA-resistant species CaCPR (epsilon CaCPR470 = 54 M-1). Equations describing the time dependence of the observed ellipticity have been derived in terms of the kinetic scheme, CPS + Ca in equilibrium or formed from CaCPS in equilibrium or formed from CaCPR, in which the second equilibrium is slow compared to the first. The above assignments allow a more complete quantitative description of the changes in CD amplitudes and band shapes due to Ca2+ binding and thus facilitate the understanding of ca2+ interactions. Calcium binds to 0.93 Ca2+ site/25 500 Mr in CaCPS with a Kd for Ca2+ = 2.1 x 10(-3) M at pH 5.3 and 25 degrees C. The interaction of Ca2+ with CPS to form CaCPS occurs at two equivalent and noninteracting S2 sites each present on separate subunits of the Con A dimer. Furthermore, the rate constant describing the rate of formation of CaCPR was determined.
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PMID:Quantitative analyses of calcium-induced spectral changes in extrinsic Cotton effects of cobalt-substituted concanavalin A. 744 79

A correlation was found between mitochondrial matrix free magnesium ([Mg2+]m), measured by means of the fluorescent indicator Mag-Fura-2, and citrulline synthesis in rat liver mitochondria. The variation of [Mg2+]m from 0.05 to 1.7 mM by changes in external Mg2+, induced a 20 +/- 8.5% increase in the rate of citrulline synthesis, whereas a further increase of [Mg2+]m to 3.3 mM induced a return to basal values. The increase in [Mg2+]m, as well as the diminution of external pH, also promoted an elevation of matrix free Ca2+ ([Ca2+]m). An increase in [Ca2+]m, at constant [Mg2+]m and pH, resulted in a 3-fold stimulation of citrulline synthesis. The data suggest that [Mg2+]m may modulate the rate of citrulline synthesis through a direct interaction with carbamoyl-phosphate synthase I (ammonia) and, indirectly, by changing the levels of matrix Ca2+.
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PMID:Effect of intramitochondrial Mg2+ on citrulline synthesis in rat liver mitochondria. 904 47

Since various secretory stimuli regulate not only secretion but also protein, RNA, and DNA syntheses in salivary glands, we evaluated the effect of secretory stimuli on the phosphorylation state of CREB (cAMP response element-binding protein). Isoproterenol, forskolin, and CPS-cAMP markedly stimulated the phosphorylation of CREB in parotid acinar cells, and PKA inhibitors H-8 and H-89 dose-dependently inhibited it. In contrast, carbachol (CCH) and A23187 decreased CREB phosphorylation, but CCH did not decrease it in the absence of extracellular Ca2+. Although protein phosphatase inhibitor calyculin A alone markedly increased the phosphorylation, it could not prevent CCH-induced dephosphorylation of CREB. CaM kinase IV, a putative protein kinase for CREB in response to Ca2+ elevation, was undetectable in parotid acinar cells.
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PMID:Regulation of CREB phosphorylation by cAMP and Ca2+ in parotid acinar cells. 935 75

Composition and amount of 45Ca2+-binding proteins in the inner membrane fraction of rat liver and Zajdela hepatoma mitochondria were determined. In the inner membrane of liver mitochondria, three major 45Ca2+-binding polypeptides: a protein of approximately 130 kDa (carbamoyl-phosphate synthetase), a glycoprotein of 43-44 kDa (previously considered as the calcium uniporter), and 29-30 kDa protein were found. These components were absent (130 kDa component) or relatively reduced (43-44 kDa and 29-30 kDa components) in the inner membrane of hepatoma mitochondria. Previously unknown low molecular mass polypeptides, having very high Ca2+-binding ability, were found in the inner membrane of hepatoma mitochondria. One of them might be the natural Ca2+-binding inhibitor of H+-ATPase.
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PMID:Calcium binding to polypeptides of rat liver and Zajdela hepatoma mitochondrial inner membranes. 950 39

Protein S from Myxococcus xanthus is a member of the beta gamma-crystallin superfamily. Its N and C-terminal domains (NPS and CPS, respectively) show a high degree of structural similarity and possess the capacity to bind two calcium ions per domain. For NPS, their positions were determined by X-ray diffraction at 1.8 A resolution, making use of molecular replacement with the NMR structure as search model. The overall topology of NPS is found to be practically the same as in complete protein S. In natural protein S, the domains fold independently, with a significant increase in stability and cooperativity of folding in the presence of Ca2+. The recombinant isolated domains are stable monomers which do not show any tendency to combine to "nicked" full-length protein S. In order to investigate the stability and folding of natural protein S and its isolated domains, spectroscopic techniques were applied, measuring the reversible urea and temperature-induced unfolding transitions at varying pH. The increment of Ca2+ to the free energy of stabilization amounts to -10 and -5 kJ/mol for NPS and CPS, respectively. For both NPS and CPS, in the absence and in the presence of 3 mM CaCl2, the two-state model is valid. Comparing DeltaGU-->N for CPS (-21 kJ/mol at pH 7, liganded with Ca2+) with its increment in the intact two-domain protein, the stability of the isolated domain turns out to be decreased in a pH-dependent manner. In contrast, the stability of Ca2+-loaded NPS (DeltaGU-->N=-31 kJ/mol, pH 7) is nearly unchanged down to pH 2 where Ca2+ is released (DeltaGU-->N=-26 kJ/mol, pH 2). In intact protein S, the N-terminal domain is destabilized relative to NPS. Evidently, apart from Ca2+ binding, well-defined domain interactions contribute significantly to the overall stability of intact protein S.
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PMID:The domains of protein S from Myxococcus xanthus: structure, stability and interactions. 1006 14

The degradation of rat hepatic carbamoyl phosphate synthetase I (CPS) by calcium-activated thiol protease (calpain II) isolated from the same tissue was evaluated in vitro. Calpain was purified as a heterodimer containing subunits of 72-kDa (catalytic) and 29-kDa (regulatory). The identity of this protease as calpain II was confirmed by its dependence on calcium in the 2-4 mM range for maximal activity (525 microM calcium required for half-maximal activity) and reactivity with anti-calpain II antibody on Western blots. Calpain II was not activated (<10%) by Mg2+ or Mn2+. CPS degradation was monitored by discontinuous sodium dodecyl sulfate-polyacrylamide slab gel electrophoresis (SDS-PAGE) and CPS fragments characterized with Western blotting with an anti-CPS antibody. Exposure of CPS (160-kDa) to calpain II resulted in the generation of single and limited degradation product of approximately 136-kDa. The smaller CPS fragment (approximately 24-kDa) appears unstable since it was not detected under these conditions. In contrast, the larger 136-kDa CPS fragment was quite stable despite extended incubation with calpain II (up to 60 min). Two-dimensional electrophoretic analysis (isoelectric focusing IEF/SDS-PAGE) revealed that the 136-kDa CPS fragment focused at more acidic isoelectric point (pI) than the parent molecule (pI range 5.95-6.35 vs 6.35-6.75, respectively). Based on the size and acidic pI shift of the degradation fragment, the calpain-susceptible site most likely involves removal of the positively-charged C-terminus of CPS. The potential significance of these findings to physiological regulation of CPS by calpain is discussed.
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PMID:Limited degradation of carbamoyl phosphate synthetase I by calcium-activated protease (calpain): electrophoretic evidence for removal of the C-terminal N-acetylglutamate regulatory domain. 1050 40


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