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Table 2 Kinetic parameters of the inwardly directed transport of Gly-Gln via the zebrafish PepT1a (Slc15a1a) and zebrafish PepT1b (Slc15a1b) measured in two-electrode voltage clamp experiments

From: The peptide transporter 1a of the zebrafish Danio rerio, an emerging model in nutrigenomics and nutrition research: molecular characterization, functional properties, and expression analysis

 − 60 mV− 120 mV 
pHNeutral form (%)K0.5 (mmol/L)Imax (nA)Imax/K0.5 (nA/mmol/L)K0.5 (mmol/L)Imax (nA)Imax/K0.5 (nA/mmol/L)Oocytes/batches (n/N)
PepT1a
 6.598.40.24 ± 0.07− 75.76 ± 6.04316.370.45 ± 0.19− 157.39 ± 21.48350.819/3
 7.683.06.92 ± 2.34− 169.57 ± 43.7524.513.61 ± 0.73− 378.82 ± 53.08105.0214/3
PepT1b
 6.598.40.13 ± 0.02− 195.73 ± 8.891535.320.13 ± 0.02− 396.24 ± 22.213032.167/1
 7.683.02.22 ± 1.04566.16 ± 212.44254.541.01 ± 0.351142.30 ± 285.341129.677/1
  1. Kinetic parameters (K0.5, Imax, and Imax/K0.5) were calculated on Xenopus laevis oocytes voltage clamped at − 60 mV and at − 120 mV and perfused with Gly-Gln in sodium chloride buffer solutions at pH 6.5 and 7.6. Values are expressed as means ± SEM of n oocytes (each oocyte represents an independent observation). Kinetic parameters were calculated by least-square fit to the logistic equation (Fig. 2). Imax/K0.5, transport efficiency