help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Originally published as Biophys J. BioFAST on October 27, 2006.
doi:10.1529/biophysj.106.092296
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
biophysj.106.092296v1
92/2/461    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gagnon, D. G.
Right arrow Articles by Lapointe, J.-Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gagnon, D. G.
Right arrow Articles by Lapointe, J.-Y.
Biophysical Journal 92:461-472 (2007)
© 2007 The Biophysical Society

Effect of Substrate on the Pre-Steady-State Kinetics of the Na+/Glucose Cotransporter

Dominique G. Gagnon, Carole Frindel and Jean-Yves Lapointe

Groupe d'étude des protéines membranaires, Université de Montréal, Montreal, Quebec, Canada

Correspondence: Address reprint requests to J.-Y. Lapointe, Groupe d'étude des protéines membranaires (GÉPROM), Université de Montréal, C.P. 6128, succ. Centre-ville, Montréal, Québec H3C 3J7, Canada. Tel.: 514-343-7046; Fax: 514-343-7146; E-mail: jean-yves.lapointe{at}umontreal.ca.

When measuring Na+/glucose cotransporter (SGLT1) activity in Xenopus oocytes with the two-electrode voltage-clamp technique, pre-steady-state currents dissipate completely in the presence of saturating {alpha}-methyl-glucose ({alpha}MG, a nonhydrolyzable glucose analog) concentrations. In sharp contrast, two SGLT1 mutants (C255A and C511A) that lack a recently identified disulfide bridge express the pre-steady-state currents in the presence of {alpha}MG. The dose-dependent effects of {alpha}MG on pre-steady-state currents were studied for wild-type (wt) SGLT1 and for the two mutants. Increases in {alpha}MG concentration reduced the total transferred charge (partially for the mutants, totally for wt SGLT1), shifted the transferred charge versus membrane potential (Q-V) curve toward positive potentials, and significantly modified the time constants of the pre-steady-state currents. A five-state kinetic model is proposed to quantitatively explain the effect of {alpha}MG on pre-steady-state currents. This analysis reveals that the reorientation of free transporter is the slowest step for wt SGLT1 either in the presence or in the absence of {alpha}MG. In contrast, the conformational change of the fully loaded mutant transporters constitutes their rate-limiting step in the presence of substrate and explains the persistence of pre-steady-state currents in this situation.




This article has been cited by other articles:


Home page
Am. J. Physiol. Cell Physiol.Home page
M. G. Blanchard, J.-P. Longpre, B. Wallendorff, and J.-Y. Lapointe
Measuring ion transport activities in Xenopus oocytes using the ion-trap technique
Am J Physiol Cell Physiol, November 1, 2008; 295(5): C1464 - C1472.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by the Biophysical Society.