» Articles » PMID: 18658227

Alternating Carrier Models of Asymmetric Glucose Transport Violate the Energy Conservation Laws

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 2008 Jul 29
PMID 18658227
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Alternating access transporters with high-affinity externally facing sites and low-affinity internal sites relate substrate transit directly to the unliganded asymmetric "carrier" (Ci) distribution. When both bathing solutions contain equimolar concentrations of ligand, zero net flow of the substrate-carrier complex requires a higher proportion of unliganded low-affinity inside sites (proportional, variant 1/KD(in)) and slower unliganded "free" carrier transit from inside to outside than in the reverse direction. However, asymmetric rates of unliganded carrier movement, kij, imply that an energy source, DeltaGcarrier = RT ln (koi/kio) = RT ln (Cin/Cout) = RT ln (KD(in)/KD(out)), where R is the universal gas constant (8.314 Joules/M/K degrees), and T is the temperature, assumed here to be 300 K degrees , sustains the asymmetry. Without this invalid assumption, the constraints of carrier path cyclicity, combined with asymmetric ligand affinities and equimolarity at equilibrium, are irreconcilable, and any passive asymmetric uniporter or cotransporter model system, e.g., Na-glucose cotransporters, espousing this fundamental error is untenable. With glucose transport via GLUT1, the higher maximal rate and Km of net ligand exit compared to net ligand entry is only properly simulated if ligand transit occurs by serial dissociation-association reactions between external high-affinity and internal low-affinity immobile sites. Faster intersite transit rates occur from lower-affinity sites than from higher-affinity sites and require no other energy source to maintain equilibrium. Similar constraints must apply to cotransport.

Citing Articles

Insight into the Mechanism of d-Glucose Accelerated Exchange in GLUT1 from Molecular Dynamics Simulations.

Domene C, Wiley B, Gonzalez-Resines S, Naftalin R Biochemistry. 2025; 64(4):928-939.

PMID: 39874207 PMC: 11840925. DOI: 10.1021/acs.biochem.4c00502.


Quantifying glucose uptake at the single cell level with confocal microscopy reveals significant variability within and across individuals.

Paprocki J, Macdonald P, Xu Y, Cheng A, Dunn T, Tetin S Sci Rep. 2025; 15(1):2661.

PMID: 39837851 PMC: 11751187. DOI: 10.1038/s41598-024-74574-3.


Energy-based bond graph models of glucose transport with SLC transporters.

Hunter P, Ai W, Nickerson D Biophys J. 2024; 124(2):316-335.

PMID: 39644093 PMC: 11788503. DOI: 10.1016/j.bpj.2024.12.006.


Structure, function and regulation of mammalian glucose transporters of the SLC2 family.

Holman G Pflugers Arch. 2020; 472(9):1155-1175.

PMID: 32591905 PMC: 7462842. DOI: 10.1007/s00424-020-02411-3.


Extracellular gating of glucose transport through GLUT 1.

Chen L, Phelix C Biochem Biophys Res Commun. 2019; 511(3):573-578.

PMID: 30824189 PMC: 6452493. DOI: 10.1016/j.bbrc.2019.02.067.


References
1.
Geck P . [Properties of an asymmetrical carrier model for the transport of sugars by human erythrocytes]. Biochim Biophys Acta. 1971; 241(2):462-72. DOI: 10.1016/0005-2736(71)90045-9. View

2.
Eskandari S, Wright E, Loo D . Kinetics of the reverse mode of the Na+/glucose cotransporter. J Membr Biol. 2005; 204(1):23-32. PMC: 3000923. DOI: 10.1007/s00232-005-0743-x. View

3.
Turner R . Kinetic analysis of a family of cotransport models. Biochim Biophys Acta. 1981; 649(2):269-80. DOI: 10.1016/0005-2736(81)90415-6. View

4.
Baker G, Naftalin R . Evidence of multiple operational affinities for D-glucose inside the human erythrocyte membrane. Biochim Biophys Acta. 1979; 550(3):474-84. DOI: 10.1016/0005-2736(79)90150-0. View

5.
Loo D, Wright E . Kinetics of steady-state currents and charge movements associated with the rat Na+/glucose cotransporter. J Biol Chem. 1995; 270(45):27099-105. DOI: 10.1074/jbc.270.45.27099. View