Analysis of protein-mediated 3-O-methylglucose transport in rat erythrocytes: rejection of the alternating conformation carrier model for sugar transport
- PMID: 2765504
- DOI: 10.1021/bi00437a012
Analysis of protein-mediated 3-O-methylglucose transport in rat erythrocytes: rejection of the alternating conformation carrier model for sugar transport
Abstract
3-O-Methylglucose (3OMG) transport in rat erythrocytes (RBCs) is mediated by a low-capacity, facilitated diffusion-type process. This study examines whether the characteristics of sugar transport in rat RBCs are consistent with the predictions of two diametric, theoretical mechanisms for sugar transport. The one-site carrier describes a transport mechanism in which sugar influx and efflux substrate binding sites are mutually exclusive. The two-site carrier describes a transport mechanism in which sugar influx and efflux substrate binding sites can exist simultaneously but may interact in a cooperative fashion when occupied by substrate. Michaelis and velocity parameters for saturable 3OMG transport in rat erythrocytes at 24 degrees C were obtained from initial rate measurements of 3OMG transport. The results are incompatible with the predictions of the one-site carrier but are consistent with the predictions of a symmetric two-site carrier, displaying negligible cooperativity between substrate binding sites. This allows reduction of the two-site carrier transport equations to a form containing fewer constants than the one-site carrier equations without limiting their predictive success. While the available evidence does not prove that rat erythrocyte sugar transport is mediated by a two-site mechanism, we conclude that adoption of the formally more complex one-site model for sugar transport in rat erythrocytes is unnecessary and unwarranted. Counterflow experiments have also been performed in which the time course of radiolabeled 3OMG uptake is measured in cells containing saturating levels of 3OMG. The results of these experiments are consistent with the hypothesis [Naftalin et al. (1985) Biochim. Biophys. Acta 820, 235-249] that exchange of sugar between intracellular compartments (cell water and hemoglobin) can be rate limiting for transport under certain conditions.
Similar articles
-
Net sugar transport is a multistep process. Evidence for cytosolic sugar binding sites in erythrocytes.Biochemistry. 1995 Nov 28;34(47):15395-406. doi: 10.1021/bi00047a002. Biochemistry. 1995. PMID: 7492539
-
Human erythrocyte sugar transport is incompatible with available carrier models.Biochemistry. 1996 Aug 13;35(32):10411-21. doi: 10.1021/bi953077m. Biochemistry. 1996. PMID: 8756697
-
Kinetic mechanism of chlorpromazine inhibition of erythrocyte 3-O-methylglucose transport.Biochim Biophys Acta. 1983 Jan 5;727(1):213-6. doi: 10.1016/0005-2736(83)90387-5. Biochim Biophys Acta. 1983. PMID: 6824652
-
Expression of substrate specificity in facilitated transport systems.J Membr Biol. 1990 Jul;117(1):69-78. doi: 10.1007/BF01871566. J Membr Biol. 1990. PMID: 2205724 Review.
-
Modeling membrane transport.Adv Food Nutr Res. 1996;40:243-62. doi: 10.1016/s1043-4526(08)60033-9. Adv Food Nutr Res. 1996. PMID: 8858819 Review.
Cited by
-
Sequence determinants of GLUT1-mediated accelerated-exchange transport: analysis by homology-scanning mutagenesis.J Biol Chem. 2012 Dec 14;287(51):42533-44. doi: 10.1074/jbc.M112.369587. Epub 2012 Oct 23. J Biol Chem. 2012. PMID: 23093404 Free PMC article.
-
ATP-dependent sugar transport complexity in human erythrocytes.Am J Physiol Cell Physiol. 2007 Feb;292(2):C974-86. doi: 10.1152/ajpcell.00335.2006. Epub 2006 Aug 23. Am J Physiol Cell Physiol. 2007. PMID: 16928769 Free PMC article.
-
Comparative characterization of hexose transporters of Plasmodium knowlesi, Plasmodium yoelii and Toxoplasma gondii highlights functional differences within the apicomplexan family.Biochem J. 2002 Dec 15;368(Pt 3):923-9. doi: 10.1042/BJ20021189. Biochem J. 2002. PMID: 12238947 Free PMC article.
-
AR-C155858 is a potent inhibitor of monocarboxylate transporters MCT1 and MCT2 that binds to an intracellular site involving transmembrane helices 7-10.Biochem J. 2010 Jan 15;425(3):523-30. doi: 10.1042/BJ20091515. Biochem J. 2010. PMID: 19929853 Free PMC article.
-
alpha- and beta-monosaccharide transport in human erythrocytes.Am J Physiol Cell Physiol. 2009 Jan;296(1):C151-61. doi: 10.1152/ajpcell.00359.2008. Epub 2008 Nov 5. Am J Physiol Cell Physiol. 2009. PMID: 18987250 Free PMC article.