Literature DB >> 6318727

Determination of Michaelis parameters from differentials of progress curves.

L C Petersen.   

Abstract

First differentials of progress curves are easily obtainable in many enzyme assay systems. Such curves may be more readily applicable to kinetic analysis than are the usual progress curves. The theory for this approach is developed, and simple graphical procedures for the determination of Michaelis parameters are indicated. By using an electronic differentiator device the application of the method is demonstrated on the kinetics of three different serine proteinases with various synthetic substrates. Whenever the steady-state concentration of an intermediate of the reaction is proportional to the rate, the transition of this intermediate in substrate-depletion experiments may be analysed in similar terms. This is demonstrated with cytochrome c oxidase kinetics. A number of other possible applications are discussed.

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Year:  1983        PMID: 6318727      PMCID: PMC1152440          DOI: 10.1042/bj2150589

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


  14 in total

1.  The use of the direct linear plot for determining initial velocities.

Authors:  A Cornish-Bowden
Journal:  Biochem J       Date:  1975-08       Impact factor: 3.857

2.  Preparation of cytochrome oxidase from beef heart.

Authors:  C R Hartzell; H Beinert; B F van Gelder; T E King
Journal:  Methods Enzymol       Date:  1978       Impact factor: 1.600

3.  Control of respiration in isolated mitochondria: quantitative evaluation of the dependence of respiratory rates on [ATP], [ADP], and [Pi].

Authors:  A Holian; C S Owen; D F Wilson
Journal:  Arch Biochem Biophys       Date:  1977-05       Impact factor: 4.013

4.  Hydrophobic interactions in the trypsin active center. The sensitivity of the hydrophobic binding site to side chain modifications in competitive inhibitors of the amidinium type.

Authors:  M Mares-Guia
Journal:  Arch Biochem Biophys       Date:  1968-09-20       Impact factor: 4.013

5.  Comparative studies on the inhibition of trypsin, plasmin, and thrombin by derivatives of benzylamine and benzamidine.

Authors:  F Markwardt; H Landmann; P Walsmann
Journal:  Eur J Biochem       Date:  1968-12-05

6.  Effect of monovalent cations on the heparin-enhanced antithrombin III/thrombin reaction.

Authors:  M J Griffith; G Beavers; H S Kingdon; R L Lundblad
Journal:  Thromb Res       Date:  1980 Jan 1-15       Impact factor: 3.944

7.  Adsorption to fibrin of native fragments of known primary structure from human plasminogen.

Authors:  S Thorsen; I Clemmensen; L Sottrup-Jensen; S Magnusson
Journal:  Biochim Biophys Acta       Date:  1981-05-29

8.  Kinetic analysis of progress curves.

Authors:  B A Orsi; K F Tipton
Journal:  Methods Enzymol       Date:  1979       Impact factor: 1.600

9.  Steady-state kinetics of plasmin- and trypsin-catalysed hydrolysis of a number of tripeptide-p-nitroanilides.

Authors:  U Christensen; H H Ipsen
Journal:  Biochim Biophys Acta       Date:  1979-08-15

10.  Kinetics of plasmin inhibition in the presence of a synthetic tripeptide substrate. The reaction with pancreatic trypsin inhibitor and two forms of alpha 2-plasmin inhibitor.

Authors:  L C Petersen; I Clemmensen
Journal:  Biochem J       Date:  1981-10-01       Impact factor: 3.857

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