Literature DB >> 6870821

Use of the F test for determining the degree of enzyme-kinetic and ligand-binding data. A Monte Carlo simulation study.

F J Burguillo, A J Wright, W G Bardsley.   

Abstract

1. Initial-rate data were simulated for 13 representative enzyme mechanisms with the use of several distributions of rate constants in order to locate conditions leading to v([S]) curves in physiological ranges of substrate concentration. 2. In all, 420 sets of such v([S]) curves were generated with the use of several choices of substrate concentration range (two, three or four orders of magnitude), number of experimental points (10, 15 or 20), error on v (5-10%) and standard deviation on v (5-9%) in order to simulate experimental results in a number of possible ways. 3. Curve-fitting was carried out to rational functions of degree 1:1, 2:2, . . ., 5:5 until there was no statistically significant decrease in the sum of weighted squared residuals as judged by the F test at 95% and 99% confidence levels. 4. It was checked whether the non-linear regression program had located a good minimum in the sum of squares by also fitting the data with the correct values of parameters as starting estimates. 5. A similar procedure was adopted with 110 sets of binding data simulated for 11 models, and the F test was used to see if fractional-saturation data generated by a binding polynomial of order n could be adequately fitted by one of order m, m less than n. 6. From the 530 simulations the F test was successful in fixing the correct degree with a probability of 0.62 at the 95% confidence level, but this fell with increase in degree as follows: 1:1 (0.98), 2:2 (0.71), 3:3 (0.43) and 4:4 (0.34), the first numbers being the degree of the rate equation and those in parentheses referring to the 95% confidence level. 7. It made little difference whether the 95% or the 99% confidence level was consulted, as there were very few borderline cases. 8. The chance of detecting deviations from Michaelis-Menten kinetics, i.e. terms of at least second-order in a rate equation of degree n:n, n greater than 1, was estimated to be about 0.8. 9. The probability of the F test leading to a spurious result due to error in the data was found to be about 0.04. 10. The probability with which 4:4 mechanisms can lead to v([S]) plots with no, one, two or three turning points was computed, and it was established that there is a small but finite chance that the increase in degree that occurs in some mechanisms when ES in equilibrium EP interconversions are explicitly allowed for can be detected by the F test.

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Year:  1983        PMID: 6870821      PMCID: PMC1154325          DOI: 10.1042/bj2110023

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


  31 in total

1.  ON THE NATURE OF ALLOSTERIC TRANSITIONS: A PLAUSIBLE MODEL.

Authors:  J MONOD; J WYMAN; J P CHANGEUX
Journal:  J Mol Biol       Date:  1965-05       Impact factor: 5.469

2.  The quantitative analysis of ligand binding and initial-rate data for allosteric and other complex enzyme mechanisms.

Authors:  W G Bardsley
Journal:  Biochem J       Date:  1976-01-01       Impact factor: 3.857

3.  Steady-state kinetic studies of the negative co-operativity and flip-flop mechanism for Escherichia coli alkaline phosphatase.

Authors:  R D Waight; P Leff; W G Bardsley
Journal:  Biochem J       Date:  1977-12-01       Impact factor: 3.857

4.  A computer system for analysis and modeling of multiple pathoway enzyme mechanisms.

Authors:  C F Lam; N Schatz; D Priest
Journal:  Comput Biol Med       Date:  1977-07       Impact factor: 4.589

5.  Some examples of the use of computer-produced contour plots in the fitting of enzyme rate equations to reaction-velocity measurements.

Authors:  J H Ottaway; D K Apps
Journal:  Biochem J       Date:  1972-12       Impact factor: 3.857

6.  The structure of steady-state enzyme kinetic equations: a graph-theoretical algorithm for obtaining conditions for reduction in degree by common-factor cancellation.

Authors:  E P Whitehead
Journal:  J Theor Biol       Date:  1979-10-07       Impact factor: 2.691

7.  Some mathematical results concerning Hessians of binding polynomials and co-operativity coefficients.

Authors:  W G Bardsley; R Woolfson; R M Wood
Journal:  J Theor Biol       Date:  1980-07-07       Impact factor: 2.691

8.  Deviations from Michaelis-Menten kinetics. Computation of the probabilities of obtaining complex curves from simple kinetic schemes.

Authors:  F Solano-Muñoz; P B McGinlay; R Woolfson; W G Bardsley
Journal:  Biochem J       Date:  1981-01-01       Impact factor: 3.857

9.  Fitting kinetic data for two independent saturable terms by MULTIFIT II, a general purpose curve fitting program in FORTRAN IV.

Authors:  R H Matthews; J O Alben
Journal:  J Theor Biol       Date:  1978-05-22       Impact factor: 2.691

10.  Mechanism of action of D-glyceraldehyde-3-phosphate dehydrogenase.

Authors:  M Feraudi; M Kohlmeier; W Glaser; T Keleti
Journal:  Acta Biochim Biophys Acad Sci Hung       Date:  1977
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  9 in total

1.  The molybdoenzymes xanthine oxidase and aldehyde oxidase contain fast- and slow-DTNB reacting sulphydryl groups.

Authors:  F Cabré; M Cascante; E I Canela
Journal:  J Protein Chem       Date:  1992-10

2.  A kinetic study of the suicide inactivation of an enzyme measured through coupling reactions. Application to the suicide inactivation of tyrosinase.

Authors:  J Escribano; J Tudela; F Garcia-Carmona; F Garcia-Canovas
Journal:  Biochem J       Date:  1989-09-01       Impact factor: 3.857

3.  The non-Michaelian action of thrombin on peptide p-nitroanilide substrates.

Authors:  C Izquierdo; F J Burguillo; W G Bardsley
Journal:  Biochem J       Date:  1987-04-15       Impact factor: 3.857

4.  A computer program for enzyme kinetics that combines model discrimination, parameter refinement and sequential experimental design.

Authors:  R Franco; M T Gavaldà; E I Canela
Journal:  Biochem J       Date:  1986-09-15       Impact factor: 3.857

5.  Robust regression of enzyme kinetic data.

Authors:  A Cornish-Bowden; L Endrenyi
Journal:  Biochem J       Date:  1986-02-15       Impact factor: 3.857

6.  Kinetic studies of chicken and turkey liver mitochondrial aspartate aminotransferase.

Authors:  M Cascante; A Cortés
Journal:  Biochem J       Date:  1988-03-15       Impact factor: 3.857

7.  Comparison of the Akaike Information Criterion, the Schwarz criterion and the F test as guides to model selection.

Authors:  T M Ludden; S L Beal; L B Sheiner
Journal:  J Pharmacokinet Biopharm       Date:  1994-10

8.  Kinetic mechanism of chicken liver xanthine dehydrogenase.

Authors:  P Bruguera; A Lopez-Cabrera; E I Canela
Journal:  Biochem J       Date:  1988-01-01       Impact factor: 3.857

9.  Evaluation of a flavonoids library for inhibition of pancreatic α-amylase towards a structure-activity relationship.

Authors:  Carina Proença; Marisa Freitas; Daniela Ribeiro; Sara M Tomé; Eduardo F T Oliveira; Matilde F Viegas; Alberto N Araújo; Maria J Ramos; Artur M S Silva; Pedro A Fernandes; Eduarda Fernandes
Journal:  J Enzyme Inhib Med Chem       Date:  2019-12       Impact factor: 5.051

  9 in total

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