Electrogenic properties of the sodium-alanine cotransporter in pancreatic acinar cells: II. Comparison with transport models
- PMID: 3560198
- DOI: 10.1007/BF01871192
Electrogenic properties of the sodium-alanine cotransporter in pancreatic acinar cells: II. Comparison with transport models
Abstract
In this paper, the results of the preceding electrophysiological study of sodium-alanine cotransport in pancreatic acinar cells are compared with kinetic models. Two different types of transport mechanisms are considered. In the "simultaneous" mechanism the cotransporter C forms a ternary complex NCS with Na+ and the substrate S; coupled transport of Na+ and S involves a conformational transition between states NC'S and NC"S with inward- and outward-facing binding sites. In the "consecutive" (or "ping-pong") mechanism, formation of a ternary complex is not required; coupled transport occurs by an alternating sequence of association-dissociation steps and conformational transitions. It is shown that the experimentally observed alanine- and sodium-concentration dependence of transport rates is consistent with the predictions of the "simultaneous" model, but incompatible with the "consecutive" mechanism. Assuming that the association-dissociation reactions are not rate-limiting, a number of kinetic parameters of the "simultaneous" model can be estimated from the experimental results. The equilibrium dissociation constants of Na+ and alanine at the extracellular side are determined to be K"N less than or equal to 64 mM and K"S less than or equal to 18 mM. Furthermore, the ratio K"N/KS"N of the dissociation constants of Na+ from the binary (NC) and the ternary complex (NCS) at the extracellular side is estimated to be less than or equal to 6. This indicates that the binding sequence of Na+ and S to the transporter is not ordered. The current-voltage behavior of the transporter is analyzed in terms of charge translocations associated with the single-reaction steps. The observed voltage-dependence of the half-saturation concentration of sodium is consistent with the assumption that a Na+ ion that migrates from the extracellular medium to the binding site has to traverse part of the transmembrane voltage.
Similar articles
-
Electrogenic properties of the sodium-alanine cotransporter in pancreatic acinar cells: I. Tight-seal whole-cell recordings.J Membr Biol. 1986;94(2):99-115. doi: 10.1007/BF01871191. J Membr Biol. 1986. PMID: 3560201
-
Kinetics of the Na+/alanine cotransporter in pancreatic acinar cells.Biochim Biophys Acta. 1988 Apr 7;939(2):179-88. doi: 10.1016/0005-2736(88)90061-2. Biochim Biophys Acta. 1988. PMID: 3355814
-
Na+-coupled alanine transport in LLC-PK1 cells: the relationship between the Km for Na+ at low [Alanine] and potential dependence for the system.J Membr Biol. 1998 Oct 1;165(3):275-82. doi: 10.1007/s002329900441. J Membr Biol. 1998. PMID: 9767681
-
Bacterial transporters: charge translocation and mechanism.Biochim Biophys Acta. 2009 Jun;1787(6):706-13. doi: 10.1016/j.bbabio.2009.02.002. Epub 2009 Feb 11. Biochim Biophys Acta. 2009. PMID: 19366604 Review.
-
Forging the link between structure and function of electrogenic cotransporters: the renal type IIa Na+/Pi cotransporter as a case study.Prog Biophys Mol Biol. 2002 Nov;80(3):69-108. doi: 10.1016/s0079-6107(02)00015-9. Prog Biophys Mol Biol. 2002. PMID: 12379267 Review.
Cited by
-
Voltage-clamp studies of the Na+/glucose cotransporter cloned from rabbit small intestine.Pflugers Arch. 1991 Mar;418(1-2):79-85. doi: 10.1007/BF00370455. Pflugers Arch. 1991. PMID: 2041729
-
Voltage and cosubstrate dependence of the Na-HCO3 cotransporter kinetics in renal proximal tubule cells.Biophys J. 1998 Aug;75(2):810-24. doi: 10.1016/S0006-3495(98)77570-8. Biophys J. 1998. PMID: 9675182 Free PMC article.
-
Transport of potassium in Chara australis: II. Kinetics of a symport with sodium.J Membr Biol. 1990 May;115(2):129-43. doi: 10.1007/BF01869452. J Membr Biol. 1990. PMID: 2355393
-
GAT1 (GABA:Na+:Cl-) cotransport function. Steady state studies in giant Xenopus oocyte membrane patches.J Gen Physiol. 1999 Sep;114(3):429-44. doi: 10.1085/jgp.114.3.429. J Gen Physiol. 1999. PMID: 10469733 Free PMC article.
-
Voltage dependence of sodium-calcium exchange: predictions from kinetic models.J Membr Biol. 1987;99(1):1-11. doi: 10.1007/BF01870617. J Membr Biol. 1987. PMID: 2448470