Literature DB >> 6320172

Cytosolic Ca2+-dependent neutral proteinases from rabbit liver: activation of the proenzymes by Ca2+ and substrate.

S Pontremoli, E Melloni, F Salamino, B Sparatore, M Michetti, B L Horecker.   

Abstract

Two neutral Ca2+-dependent proteinases, differing in molecular size, have been isolated from rabbit liver. Both are recovered as inactive proenzymes that can be converted to the active forms by high (0.1-1.0 mM) concentrations of Ca2+ in the absence of substrate or, in the presence of a protein substrate, by low (1-5 microM) concentrations of Ca2+. The activated proteinases required only 1-5 microM Ca2+ for maximal activity. Substrates hydrolyzed were denatured globin, globin, casein, and to a lesser extent, several extracellular proteins; no digestion was observed with several intracellular cytosolic enzymes tested. Only those proteins that served as substrates were capable of promoting conversion of the proenzymes to the active low-Ca2+-requiring proteinases.

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Year:  1984        PMID: 6320172      PMCID: PMC344608          DOI: 10.1073/pnas.81.1.53

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  21 in total

1.  The isolation and kinetics of two forms of fumarase from torula yeast.

Authors:  S HAYMAN; R A ALBERTY
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2.  Studies on a cyclic nucleotide-independent protein kinase and its proenzyme in mammalian tissues. II. Proenzyme and its activation by calcium-dependent protease from rat brain.

Authors:  M Inoue; A Kishimoto; Y Takai; Y Nishizuka
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3.  Studies of a calcium-activated neutral protease from chicken skeletal muscle. I. Purification and characterization.

Authors:  S Ishiura; H Murofushi; K Suzuki; K Imahori
Journal:  J Biochem       Date:  1978-07       Impact factor: 3.387

4.  Rabbit liver fructose 1,6-diphosphatase. Properties of the native enzyme and their modification by subtilisin.

Authors:  S Traniello; E Melloni; S Pontremoli; C L Sia; R L Horecker
Journal:  Arch Biochem Biophys       Date:  1972-03       Impact factor: 4.013

5.  Use of fluorescamine in the chromatographic analysis of peptides from proteins.

Authors:  N Nakai; C Y Lai; B L Horecker
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6.  Activation of skeletal muscle phosphorylase kinase by Ca2+. II. Identification of the kinase activating factor as a proteolytic enzyme.

Authors:  R B Huston; E G Krebs
Journal:  Biochemistry       Date:  1968-06       Impact factor: 3.162

7.  Autolysis of calcium-activated neutral protease of chicken skeletal muscle.

Authors:  K Suzuki; S Tsuji; S Ishiura; Y Kimura; S Kubota; K Imahori
Journal:  J Biochem       Date:  1981-12       Impact factor: 3.387

8.  Cooperation between soluble and membrane-bound proteinases in the degradation of beta-hemoglobin chains in intact human erythrocytes.

Authors:  E Melloni; F Salamino; B Sparatore; M Michetti; S Pontremoli
Journal:  Arch Biochem Biophys       Date:  1982-07       Impact factor: 4.013

9.  Limited autolysis reduces the Ca2+ requirement of a smooth muscle Ca2+-activated protease.

Authors:  D R Hathaway; D K Werth; J R Haeberle
Journal:  J Biol Chem       Date:  1982-08-10       Impact factor: 5.157

10.  A Ca2+-activated protease possibly involved in myofibrillar protein turnover. Purification from porcine muscle.

Authors:  W R Dayton; D E Goll; M G Zeece; R M Robson; W J Reville
Journal:  Biochemistry       Date:  1976-05-18       Impact factor: 3.162

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  12 in total

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2.  Calpain is a mediator of preservation-reperfusion injury in rat liver transplantation.

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3.  The effects of a calcium dependent protease on the ultrastructure and contractile mechanics of skinned uterine smooth muscle.

Authors:  J R Haeberle; S A Coolican; A Evan; D R Hathaway
Journal:  J Muscle Res Cell Motil       Date:  1985-06       Impact factor: 2.698

4.  Stimulatory effect of regucalcin on proteolytic activity in rat renal cortex cytosol: involvement of thiol proteases.

Authors:  T Baba; M Yamaguchi
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5.  A dual role for the Ca2+-requiring proteinase in the degradation of hemoglobin by erythrocyte membrane proteinases.

Authors:  S Pontremoli; E Melloni; B Sparatore; M Michetti; B L Horecker
Journal:  Proc Natl Acad Sci U S A       Date:  1984-11       Impact factor: 11.205

6.  Proactivator-dependent activation of procollagenase induced by treatment with EGTA.

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Journal:  Biochem J       Date:  1986-08-01       Impact factor: 3.857

7.  Isolation and Partial Purification of Prophenoloxidase from Daucus carota L. Cell Cultures.

Authors:  K Söderhäll; I Carlberg; T Eriksson
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8.  Characterization of regucalcin effect on proteolytic activity in rat liver cytosol: relation to cysteinyl-proteases.

Authors:  M Yamaguchi; N Nishina
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9.  Parathymosin alpha: a peptide from rat tissues with structural homology to prothymosin alpha.

Authors:  A A Haritos; S B Salvin; R Blacher; S Stein; B L Horecker
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

10.  Calcium-binding protein regucalcin increases calcium-independent proteolytic activity in rat liver cytosol.

Authors:  M Yamaguchi; H Tai
Journal:  Mol Cell Biochem       Date:  1992-05-13       Impact factor: 3.396

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