In this note, we analyze ionic transport in lipid model bilayers across pre-existing transmembrane water pores that represent a facilitated pathway for the movement of single inorganic ions and offer the possibility to overcome the Born charging energy. Following the statistical rate approach recently proposed by Skinner et al., we present a kinetic model that involves the formation of a pore-ion complex at the membrane-solution interface and its diffusion through the membrane core. The overall process is described as due to four kinetic reactions consisting respectively in the ion-pore coupling and ion-pore uncoupling (treated as second-order reactions) and translocation of free- and ion-occupied pore through the membrane, treated as simple first-order reactions. The modified kinetic approach presented here may be regarded as a generallization of an our previous work where the pore diffusion, either in presence or in absence of an ion was treated with the same rate constants. This modification should allow a better description of the voltage-current relationships observed in lipid bilayer membranes under the influence of potential and ion concentration gradients, particularly as far as deviations from ohmic behaviour are concerned. (C) 1999 Elsevier Science B.V. All rights reserved.
Ion transport in lipid bilayer membranes through aqueous pores / Bordi, Federico; Cametti, Cesare; A., Naglier. - In: COLLOIDS AND SURFACES. A, PHYSICOCHEMICAL AND ENGINEERING ASPECTS. - ISSN 0927-7757. - 159:2-3(1999), pp. 231-237. (Intervento presentato al convegno Conference on Electrokinetic Phenomena tenutosi a SLAZBURG, AUSTRIA nel APR 14-17, 1998) [10.1016/s0927-7757(99)00277-0].
Ion transport in lipid bilayer membranes through aqueous pores
BORDI, FEDERICO;CAMETTI, Cesare;
1999
Abstract
In this note, we analyze ionic transport in lipid model bilayers across pre-existing transmembrane water pores that represent a facilitated pathway for the movement of single inorganic ions and offer the possibility to overcome the Born charging energy. Following the statistical rate approach recently proposed by Skinner et al., we present a kinetic model that involves the formation of a pore-ion complex at the membrane-solution interface and its diffusion through the membrane core. The overall process is described as due to four kinetic reactions consisting respectively in the ion-pore coupling and ion-pore uncoupling (treated as second-order reactions) and translocation of free- and ion-occupied pore through the membrane, treated as simple first-order reactions. The modified kinetic approach presented here may be regarded as a generallization of an our previous work where the pore diffusion, either in presence or in absence of an ion was treated with the same rate constants. This modification should allow a better description of the voltage-current relationships observed in lipid bilayer membranes under the influence of potential and ion concentration gradients, particularly as far as deviations from ohmic behaviour are concerned. (C) 1999 Elsevier Science B.V. All rights reserved.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.