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PMID: 4715343 Published · ppublish English Journal Article

The asymmetry of the facilitated transfer system for hexoses in human red cells and the simple kinetics of a two component model.

The Journal of physiology ·Vol. 231 ·No. 1 ·1973-05-00 ·Pages 143-65

Baker GF, Widdas WF

Abstract

1. 4, 6-O-Ethylidene-alpha-D-glucopyranose (ethylidene glucose) has been used to study the competitive inhibition of glucose exchange fluxes when the reagent was (i) inside the cells and (ii) on the outside.2. 50% inhibition of glucose exchange at 20 mM and 16 degrees C required 200 mM ethylidene glucose when on the inside in contrast to 25-30 mM when on the outside.3. The inhibitions at different inhibitor/glucose concentration ratios were measured and analysis of the data suggested that the half-saturation constant for ethylidene glucose was 6 times that for glucose inside the cell as against 1.5 outside. The analysis, however, suggested an asymmetry in respect to the affinities for glucose of approximately ten-fold and this would make the asymmetry towards ethylidene glucose forty-fold.4. Such asymmetries make it necessary to consider a transfer mechanism for sugars with different components on the outer and inner membrane interfaces and simple kinetics for a two component system have been developed and used for analysing the experimental data quantitatively.5. The kinetic similarities to and difference from the kinetics of a simple mobile carrier and those of some more recent models are briefly discussed.

MeSH Terms
Biological Transport, Active/drug effects Carbon Isotopes Cell Membrane Permeability/drug effects Culture Media Diffusion Disaccharides/pharmacology Erythrocytes/metabolism Extracellular Space Glucose/metabolism Humans In Vitro Techniques Kinetics Models, Biological Osmotic Pressure
Chemicals
Carbon Isotopes Culture Media Disaccharides Glucose
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Baker G F
Widdas W F
References (19)
19 references, click to expand
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Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1973-05-00
Pages
143-65
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1350442
Subset
IM
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