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dc.contributor.authorBlodgett, David M.
dc.contributor.authorCarruthers, Anthony
dc.date2022-08-11T08:08:54.000
dc.date.accessioned2022-08-23T16:11:25Z
dc.date.available2022-08-23T16:11:25Z
dc.date.issued2004-05-04
dc.date.submitted2008-03-21
dc.identifier.citationBlood Cells Mol Dis. 2004 May-Jun;32(3):401-7. <a href="http://dx.doi.org/10.1016/j.bcmd.2004.01.015">Link to article on publisher's site</a>
dc.identifier.issn1079-9796 (Print)
dc.identifier.doi10.1016/j.bcmd.2004.01.015
dc.identifier.pmid15121099
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33159
dc.description.abstractThe 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.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=15121099&dopt=Abstract ">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.bcmd.2004.01.015
dc.subject3-O-Methylglucose; Adenosine Triphosphate; Biological Transport; Carbohydrate Metabolism; Cell Membrane Permeability; Erythrocytes; Humans; Kinetics; Models, Chemical; Temperature
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleConventional transport assays underestimate sugar transport rates in human red cells
dc.typeJournal Article
dc.source.journaltitleBlood cells, molecules and diseases
dc.source.volume32
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/17
dc.identifier.contextkey467867
html.description.abstract<p>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.</p>
dc.identifier.submissionpathgsbs_sp/17
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages401-7


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