Literature DB >> 1895338

Analysis of kinetic data in transport studies: new insights from kinetic studies of Na(+)-D-glucose cotransport in human intestinal brush-border membrane vesicles using a fast sampling, rapid filtration apparatus.

C Malo1, A Berteloot.   

Abstract

Using the fast sampling, rapid filtration apparatus (FSRFA) recently developed in our laboratory (Berteloot et al., 1991, J. Membrane Biol. 122:111-125), we have studied the kinetic characteristics of Na(+)-D-glucose cotransport in brush-border membrane vesicles isolated from normal adult human jejunum. True initial rates of transport have been determined at both 20 and 35 degrees C using a dynamic approach which involves linear-regression analysis over nine time points equally spaced over 4.5 or 2.7 sec, respectively. When the tracer rate of transport was studied as a function of unlabeled substrate concentrations added to the incubation medium, a displacement curve was generated which can be analyzed by nonlinear regression using equations which take into account the competitive inhibition of tracer flux by unlabeled substrate. This approach was made imperative since at 20 degrees C, in the presence of high substrate concentrations or 1 mM phlorizin, no measurable diffusion was found and the resultant zero slope values cannot be expressed into a classical v versus S plot. All together, our results support the existence of a single Na(+)-D-glucose cotransport system in these membranes for which Na+ is mandatory for uptake. This conclusion is at variance with that of a recent report using the same preparation (Harig et al., 1989. Am J. Physiol. 256:8618-8623). Since the discrepancy seems difficult to resolve on the consideration of experimental conditions alone, we have determined the kinetic parameters of D-glucose transport using one time point measurements and linear transformations of the Michaelis-Menten equation, in order to investigate the potential problems of such a widely used procedure. Comparing these approaches, we conclude that: (i) the dynamic uptake measurements give a better understanding of the different uptake components involved: (ii) it does not matter whether a dynamic or a one time point approach is chosen to generate the uptake data provided that a nonlinear-regression analysis with proper weighting of the data points is performed; (iii) analytical procedures which rely on linearization of Michaelian process(es) are endowed with a number of difficulties which make them unsuitable to resolve multicomponent systems in transport studies. A more general procedure which uses a nonlinear-regression analysis and a displacement curve is proposed since we demonstrate that it is far superior in terms of rapidity, data interpretation, and visual information.

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Year:  1991        PMID: 1895338     DOI: 10.1007/bf01872636

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  30 in total

1.  Fast sampling, rapid filtration apparatus: principal characteristics and validation from studies of D-glucose transport in human jejunal brush-border membrane vesicles.

Authors:  A Berteloot; C Malo; S Breton; M Brunette
Journal:  J Membr Biol       Date:  1991-06       Impact factor: 1.843

2.  Kinetic evidence for heterogeneity in Na+-D-glucose cotransport systems in the normal human fetal small intestine.

Authors:  C Malo
Journal:  Biochim Biophys Acta       Date:  1988-02-18

3.  Use of nonlinear regression to analyze enzyme kinetic data: application to situations of substrate contamination and background subtraction.

Authors:  R J Leatherbarrow
Journal:  Anal Biochem       Date:  1990-02-01       Impact factor: 3.365

4.  Temperature sensitivity and substrate specificity of two distinct Na+-activated D-glucose transport systems in guinea pig jejunal brush border membrane vesicles.

Authors:  E Brot-Laroche; M A Serrano; B Delhomme; F Alvarado
Journal:  J Biol Chem       Date:  1986-05-15       Impact factor: 5.157

5.  Proximo-distal gradient of Na+-dependent D-glucose transport activity in the brush border membrane vesicles from the human fetal small intestine.

Authors:  C Malo; A Berteloot
Journal:  FEBS Lett       Date:  1987-08-10       Impact factor: 4.124

6.  Glucose transport in isolated brush border membrane from rat small intestine.

Authors:  U Hopfer; K Nelson; J Perrotto; K J Isselbacher
Journal:  J Biol Chem       Date:  1973-01-10       Impact factor: 5.157

Review 7.  Biochemistry of the Na+, D-glucose cotransporter of the small-intestinal brush-border membrane. The state of the art in 1984.

Authors:  G Semenza; M Kessler; M Hosang; J Weber; U Schmidt
Journal:  Biochim Biophys Acta       Date:  1984-09-03

8.  A simple apparatus for performing short-time (1--2 seconds) uptake measurements in small volumes; its application to D-glucose transport studies in brush border vesicles from rabbit jejunum and ileum.

Authors:  M Kessler; V Tannenbaum; C Tannenbaum
Journal:  Biochim Biophys Acta       Date:  1978-05-18

9.  Separation of two distinct Na+/D-glucose cotransport systems in the human fetal jejunum by means of their differential specificity for 3-O-methylglucose.

Authors:  C Malo
Journal:  Biochim Biophys Acta       Date:  1990-02-16

10.  Membrane potential dependency of glutamic acid transport in rabbit jejunal brush-border membrane vesicles: K+ and H+ effects.

Authors:  A Berteloot
Journal:  Biochim Biophys Acta       Date:  1986-10-23
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  31 in total

1.  Modeling of cellular arginine uptake by more than one transporter.

Authors:  Marietha J Nel; Angela J Woodiwiss; Geoffrey P Candy
Journal:  J Membr Biol       Date:  2011-11-24       Impact factor: 1.843

2.  Twelve transmembrane helices form the functional core of mammalian MATE1 (multidrug and toxin extruder 1) protein.

Authors:  Xiaohong Zhang; Xiao He; Joseph Baker; Florence Tama; Geoffrey Chang; Stephen H Wright
Journal:  J Biol Chem       Date:  2012-06-21       Impact factor: 5.157

3.  Fast sampling, rapid filtration apparatus: principal characteristics and validation from studies of D-glucose transport in human jejunal brush-border membrane vesicles.

Authors:  A Berteloot; C Malo; S Breton; M Brunette
Journal:  J Membr Biol       Date:  1991-06       Impact factor: 1.843

4.  The effect of epidermal growth factor on brush border surface area and function in the distal remnant following resection in the rabbit.

Authors:  J A Hardin; B Chung; E V O'loughlin; D G Gall
Journal:  Gut       Date:  1999-01       Impact factor: 23.059

5.  Lack of Influence of Substrate on Ligand Interaction with the Human Multidrug and Toxin Extruder, MATE1.

Authors:  Lucy J Martínez-Guerrero; Mark Morales; Sean Ekins; Stephen H Wright
Journal:  Mol Pharmacol       Date:  2016-07-14       Impact factor: 4.436

6.  Multiple mechanisms of ligand interaction with the human organic cation transporter, OCT2.

Authors:  Jaclyn N Harper; Stephen H Wright
Journal:  Am J Physiol Renal Physiol       Date:  2012-10-03

7.  Characterization of the disposition and toxicokinetics of N-butylpyridinium chloride in male F-344 rats and female B6C3F1 mice and its transport by organic cation transporter 2.

Authors:  Y Cheng; S H Wright; M J Hooth; I G Sipes
Journal:  Drug Metab Dispos       Date:  2009-01-26       Impact factor: 3.922

8.  MATE1 has an external COOH terminus, consistent with a 13-helix topology.

Authors:  Xiaohong Zhang; Stephen H Wright
Journal:  Am J Physiol Renal Physiol       Date:  2009-06-10

9.  Substrate-dependent ligand inhibition of the human organic cation transporter OCT2.

Authors:  Mathew Belzer; Mark Morales; Bhumasamudram Jagadish; Eugene A Mash; Stephen H Wright
Journal:  J Pharmacol Exp Ther       Date:  2013-05-24       Impact factor: 4.030

10.  L-glucose absorption in house sparrows (Passer domesticus) is nonmediated.

Authors:  M-H Chang; J G Chediack; E Caviedes-Vidal; W H Karasov
Journal:  J Comp Physiol B       Date:  2003-12-16       Impact factor: 2.200

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