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    Conventional transport assays underestimate sugar transport rates in human red cells

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    Authors
    Blodgett, David M.
    Carruthers, Anthony
    UMass Chan Affiliations
    Department of Biochemistry and Molecular Pharmacology
    Graduate School of Biomedical Sciences
    Document Type
    Journal Article
    Publication Date
    2004-05-04
    Keywords
    3-O-Methylglucose; Adenosine Triphosphate; Biological Transport; Carbohydrate Metabolism; Cell Membrane Permeability; Erythrocytes; Humans; Kinetics; Models, Chemical; Temperature
    Life Sciences
    Medicine and Health Sciences
    
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    Link to Full Text
    http://dx.doi.org/10.1016/j.bcmd.2004.01.015
    Abstract
    The time course of protein-mediated 3-O-methylglucose uptake by human red cells and by red cell ghosts containing or lacking 4 mM MgATP was measured at ice temperature and sub-saturating sugar levels by conventional sampling procedures and at 20 degrees C by use of a quench-flow apparatus. The temporal resolution of the quench-flow apparatus (as fast as 5-ms sample times) was confirmed by analysis of alkaline hydrolysis of dinitrophenolacetate. Red cell sugar uptake at 4 degrees C is consistent with two processes [fast (tau = 120 s) and slow (tau = 1100 s)] that occur in series. Intracellular ATP increases the size and the rate of equilibration of the fast compartment and slows the rate of filling of the slow compartment. Red cell ghost volume and protein content are unaffected by lysis/resealing in the presence of ATP. Uptake at 20 degrees C is also consistent with two processes [fast (tau = 10 ms) and slow (tau = 15 s)] that occur in series. ATP increases the size of both compartments and the rate of filling of the small compartment at 20 degrees C. Preliminary estimates indicate that the sugar uptake capacity of human red cells at 20 degrees C is underestimated by as much as 8-fold by measuring sugar uptake over 2 s vs. 26 ms. We discuss the implications of multiphasic sugar uptake in the context of models for protein-mediated sugar transport.
    Source
    Blood Cells Mol Dis. 2004 May-Jun;32(3):401-7. Link to article on publisher's site
    DOI
    10.1016/j.bcmd.2004.01.015
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/33159
    PubMed ID
    15121099
    Related Resources
    Link to article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.bcmd.2004.01.015
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