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Transport Reversal during Heteroexchange: A Kinetic Study

It is known that secondary transporters, which utilize transmembrane ionic gradients to drive their substrates up a concentration gradient, can reverse the uptake and instead release their substrates. Unfortunately, the Michaelis-Menten kinetic scheme, which is popular in transporter studies, does n...

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Autores principales: Makarov, V., Kucheryavykh, L., Kucheryavykh, Y., Rivera, A., Eaton, M. J., Skatchkov, S. N., Inyushin, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825127/
https://www.ncbi.nlm.nih.gov/pubmed/24307897
http://dx.doi.org/10.1155/2013/683256
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author Makarov, V.
Kucheryavykh, L.
Kucheryavykh, Y.
Rivera, A.
Eaton, M. J.
Skatchkov, S. N.
Inyushin, M.
author_facet Makarov, V.
Kucheryavykh, L.
Kucheryavykh, Y.
Rivera, A.
Eaton, M. J.
Skatchkov, S. N.
Inyushin, M.
author_sort Makarov, V.
collection PubMed
description It is known that secondary transporters, which utilize transmembrane ionic gradients to drive their substrates up a concentration gradient, can reverse the uptake and instead release their substrates. Unfortunately, the Michaelis-Menten kinetic scheme, which is popular in transporter studies, does not include transporter reversal, and it completely neglects the possibility of equilibrium between the substrate concentrations on both sides of the membrane. We have developed a complex two-substrate kinetic model that includes transport reversal. This model allows us to construct analytical formulas allowing the calculation of a “heteroexchange” and “transacceleration” using standard Michaelis coefficients for respective substrates. This approach can help to understand how glial and other cells accumulate substrates without synthesis and are able to release such substrates and gliotransmitters.
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spelling pubmed-38251272013-12-04 Transport Reversal during Heteroexchange: A Kinetic Study Makarov, V. Kucheryavykh, L. Kucheryavykh, Y. Rivera, A. Eaton, M. J. Skatchkov, S. N. Inyushin, M. J Biophys Research Article It is known that secondary transporters, which utilize transmembrane ionic gradients to drive their substrates up a concentration gradient, can reverse the uptake and instead release their substrates. Unfortunately, the Michaelis-Menten kinetic scheme, which is popular in transporter studies, does not include transporter reversal, and it completely neglects the possibility of equilibrium between the substrate concentrations on both sides of the membrane. We have developed a complex two-substrate kinetic model that includes transport reversal. This model allows us to construct analytical formulas allowing the calculation of a “heteroexchange” and “transacceleration” using standard Michaelis coefficients for respective substrates. This approach can help to understand how glial and other cells accumulate substrates without synthesis and are able to release such substrates and gliotransmitters. Hindawi Publishing Corporation 2013 2013-10-26 /pmc/articles/PMC3825127/ /pubmed/24307897 http://dx.doi.org/10.1155/2013/683256 Text en Copyright © 2013 V. Makarov et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Makarov, V.
Kucheryavykh, L.
Kucheryavykh, Y.
Rivera, A.
Eaton, M. J.
Skatchkov, S. N.
Inyushin, M.
Transport Reversal during Heteroexchange: A Kinetic Study
title Transport Reversal during Heteroexchange: A Kinetic Study
title_full Transport Reversal during Heteroexchange: A Kinetic Study
title_fullStr Transport Reversal during Heteroexchange: A Kinetic Study
title_full_unstemmed Transport Reversal during Heteroexchange: A Kinetic Study
title_short Transport Reversal during Heteroexchange: A Kinetic Study
title_sort transport reversal during heteroexchange: a kinetic study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825127/
https://www.ncbi.nlm.nih.gov/pubmed/24307897
http://dx.doi.org/10.1155/2013/683256
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