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First published online on December 21, 2004.
Copyright © 2004 by The Physiological Society
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Received October 2, 2004
Revised November 1, 2004
Accepted after revision December 21, 2004

Determination of transport stoichiometry for two cation-coupled myo-inositol cotransporters: SMIT2 and HMIT

Francis Bourgeois1, Michael J Coady1, and Jean-Yves Lapointe2*

1 Université de Montréal
2 University of Montreal

* To whom correspondence should be addressed. E-mail: jean-yves.lapointe{at}umontreal.ca.

Three different mammalian myo-inositol cotransporters are currently known; two are Na+-coupled (SMIT1 and SMIT2) and one is proton-coupled (HMIT). Their transport stoichiometries have not been directly determined although significant cooperativities in the Na+ activation of SMIT1 and SMIT2 suggest that more than 1 Na+ ion drives the transport of each myo-inositol. The two techniques used here to determine transport stoichiometry take advantage of the electrogenicity of both SMIT2 and HMIT expressed in Xenopus oocytes. The first method compares the measurement of charge transferred into voltage-clamped oocytes with the simultaneous uptake of radiolabelled substrate. The second approach uses high accuracy volume measurements to determine the transport-dependent osmolyte uptake and compares it to the amount of charge transported. This method was calibrated using a potassium channel (ROMK2) and was validated with the Na+/glucose cotransporter SGLT1, which has a known stoichiometry of 2:1. Volume measurements indicated a stoichiometric ratio of 1.78 ± 0.27 ion per alpha-methyl-glucose ({alpha}MG) for SGLT1 whereas the radiotracer uptake method indicated 2.14 ± 0.05. The two methods yielded a SMIT2 stoichiometry measurement of 1.75 ± 0.30 and 1.82 ± 0.10, both in agreement with a 2 Na+:1 myo-inositol stoichiometry. For HMIT, the flux ratio was 1.02 ± 0.04 charge per myo-inositol but the volumetric method suggested 0.67 ± 0.05 charge per myo-inositol molecule. This last value is presumed to be an underestimation of the true stoichiometry of 1 proton for 1 myo-inositol due to proton exchange for osmotically active species. This hypothesis was confirmed by using SGLT1 as a proton-driven glucose cotransporter. In conclusion, despite the inherent difficulty in estimating the osmotic effect of a proton influx, the volumetric method was found valuable as it has the unique capacity of detecting unidentified transported substrates.


Key words: Co-transport • Electrophysiology • Stoichiometry




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