6533b858fe1ef96bd12b6376

RESEARCH PRODUCT

Monovalent cation conductance in Xenopus laevis oocytes expressing hCAT-3

Wolfgang GillesEllen I. ClossJohanna RuppJana F. LiewaldNicole VékonyHermann NawrathSebastian D. VulcuAlice Habermeier

subject

l-ArgininePassive transportVoltage clampHuman cationic amino acid transporter type threeBiophysicsXenopusArginineK+BiochemistryMembrane PotentialsXenopus laevisAnimalsHumansAmino acid transporterCationic Amino Acid Transporter 1Membrane potentialChromatographybiologyChemistrySodiumElectric ConductivityConductanceTransporterCell BiologyCations MonovalentNa+biology.organism_classificationRecombinant ProteinsOocytesPotassiumBiophysicsSteady state (chemistry)Cationic amino acid transporter

description

hCAT-3 (human cationic amino acid transporter type three) was investigated with both the two-electrode voltage clamp method and tracer experiments. Oocytes expressing hCAT-3 displayed less negative membrane potentials and larger voltage-dependent currents than native or water-injected oocytes did. Ion substitution experiments in hCAT-3-expressing oocytes revealed a large conductance for Na + and K + . In the presence of l-Arg, voltage-dependent inward and outward currents were observed. At symmetrical (inside/outside) concentrations of l-Arg, the conductance of the transporter increased monoexponentially with the l-Arg concentrations; the calculated Vmax and KM values amounted to 8.3 AS and 0.36 mM, respectively. The time constants of influx and efflux of [ 3 H]l-Arg, at symmetrically inside/outside l-Arg concentrations (1 mM), amounted to 79 and 77 min, respectively. The flux data and electrophysiological experiments suggest that the transport of l-Arg through hCAT-3 is symmetric, when the steady state of l-Arg flux has been reached. It is concluded that hCAT-3 is a passive transport system that conducts monovalent cations including l-Arg. The particular role of hCAT-3 in the diverse tissues remains to be elucidated. D 2004 Elsevier B.V. All rights reserved.

https://doi.org/10.1016/j.bbamem.2004.12.011