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Kinetic Models of Secondary Active Transporters.
Burtscher, Verena; Schicker, Klaus; Freissmuth, Michael; Sandtner, Walter.
Afiliação
  • Burtscher V; Institute of Pharmacology and the Gaston H. Glock Research Laboratories for Exploratory Drug Development, Center of Physiology and Pharmacology, Medical University of Vienna, 1090 Vienna, Austria. verena.burtscher@meduniwien.ac.at.
  • Schicker K; Institute of Pharmacology and the Gaston H. Glock Research Laboratories for Exploratory Drug Development, Center of Physiology and Pharmacology, Medical University of Vienna, 1090 Vienna, Austria. klaus.schicker@meduniwien.ac.at.
  • Freissmuth M; Institute of Pharmacology and the Gaston H. Glock Research Laboratories for Exploratory Drug Development, Center of Physiology and Pharmacology, Medical University of Vienna, 1090 Vienna, Austria. michael.freissmuth@meduniwien.ac.at.
  • Sandtner W; Institute of Pharmacology and the Gaston H. Glock Research Laboratories for Exploratory Drug Development, Center of Physiology and Pharmacology, Medical University of Vienna, 1090 Vienna, Austria. walter.sandtner@meduniwien.ac.at.
Int J Mol Sci ; 20(21)2019 Oct 28.
Article em En | MEDLINE | ID: mdl-31661895
ABSTRACT
Kinetic models have been employed to understand the logic of substrate transport through transporters of the Solute Carrier (SLC) family. All SLC transporters operate according to the alternate access model, which posits that substrate transport occurs in a closed loop of partial reactions (i.e., a transport cycle). Kinetic models can help to find realistic estimates for conformational transitions between individual states of the transport cycle. When constrained by experimental results, kinetic models can faithfully describe the function of a candidate transporter at a pre-steady state. In addition, we show that kinetic models can accurately predict the intra- and extracellular substrate concentrations maintained by the transporter at a steady state, even under the premise of loose coupling between the electrochemical gradient of the driving ion and of the substrate. We define the criteria for the design of a credible kinetic model of the SLC transporter. Parsimony is the guiding principle of kinetic modeling. We argue, however, that the level of acceptable parsimony is limited by the need to account for the substrate gradient established by a secondary active transporter, and for random order binding of co-substrates and substrate. Random order binding has consistently been observed in transporters of the SLC group.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sódio / Serotonina / Proteínas Carreadoras de Solutos Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sódio / Serotonina / Proteínas Carreadoras de Solutos Idioma: En Ano de publicação: 2019 Tipo de documento: Article