Literature DB >> 2363704

Kinetic analysis of regeneration by dilution of a covalently modified protein.

E T Rakitzis1.   

Abstract

An analysis of regeneration by dilution of a covalently modified protein is presented. It is shown that, when protein regeneration is realized through the intermediacy of a protein-modifying agent adsorptive complex, the reaction is described by a summation of two exponential functions of reaction time plus a constant-term equation. The conditions whereby this equation reduces to a single-exponential equation are delineated. It is shown that, when protein regeneration is described by a single-exponential function of reaction time, the first-order protein-regeneration rate constant is a function of modifying-agent concentration and also of the microscopic reaction rate constants. Accordingly, the protein-modifying agent dissociation constant (Ki), as well as the protein-covalent-modification and -regeneration, rate constants (k+2 and K-2), may be determined by an analysis of dilution-induced protein-regeneration (or enzyme-reactivation) data obtained at different dilutions of the covalently modified protein-modifying agent preparation.

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Year:  1990        PMID: 2363704      PMCID: PMC1131491          DOI: 10.1042/bj2680669

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  10 in total

1.  Kinetics and equilibrium of the inactivation of ornithine transcarbamylases by pyridoxal 5'-phosphate.

Authors:  M Marshall; P P Cohen
Journal:  J Biol Chem       Date:  1977-06-25       Impact factor: 5.157

2.  Horse liver alcohol dehydrogenase. A study of the essential lysine residue.

Authors:  S S Chen; P C Engel
Journal:  Biochem J       Date:  1975-09       Impact factor: 3.857

3.  The equilibrium position of the reaction of bovine liver glutamate dehydrogenase with pyridoxal5'-phosphate. A demonstration that covalent modification with this reagent completely abolishes catalytic activity.

Authors:  S S Chen; P C Engel
Journal:  Biochem J       Date:  1975-05       Impact factor: 3.857

4.  Kinetic analysis of protein modification reactions at equilibrium.

Authors:  E T Rakitzis
Journal:  Biochem J       Date:  1989-11-01       Impact factor: 3.857

5.  Chemical modification of arginine at the active site of the bovine erythrocyte superoxide dismutase.

Authors:  D P Malinowski; I Fridovich
Journal:  Biochemistry       Date:  1979-12-25       Impact factor: 3.162

6.  The equilibrium assumption is valid for the kinetic treatment of most time-dependent protein-modification reactions.

Authors:  K Brocklehurst
Journal:  Biochem J       Date:  1979-09-01       Impact factor: 3.857

Review 7.  Kinetics of protein modification reactions.

Authors:  E T Rakitzis
Journal:  Biochem J       Date:  1984-01-15       Impact factor: 3.857

8.  The reaction of pyridoxal 5'-phosphate with an essential lysine residue of saccharopine dehydrogenase (L-lysine-forming).

Authors:  H Ogawa; M Fujioka
Journal:  J Biol Chem       Date:  1980-08-10       Impact factor: 5.157

9.  Chemical modification of an essential lysine at the active site of enoyl-CoA reductase in fatty acid synthetase.

Authors:  A J Poulose; P E Kolattukudy
Journal:  Arch Biochem Biophys       Date:  1980-04-15       Impact factor: 4.013

10.  Role of tyrosyl and arginyl residues in rat liver microsomal stearylcoenzyme A desaturase.

Authors:  H G Enoch; P Strittmatter
Journal:  Biochemistry       Date:  1978-11-14       Impact factor: 3.162

  10 in total
  1 in total

Review 1.  Utilization of the free energy of the reversible binding of protein and modifying agent towards the rate-enhancement of protein covalent modification.

Authors:  E T Rakitzis
Journal:  Biochem J       Date:  1990-08-01       Impact factor: 3.857

  1 in total

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