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. 1997 Feb 1;17(3):960–974. doi: 10.1523/JNEUROSCI.17-03-00960.1997

Table 1.

hDAT turnover rate determined from saturation analyses of DA uptake velocity and [3H]mazindol binding to intact oocytes

DA uptake1-a [3H]mazindol binding Turnover rate
Vmax KT Bmax KD Vmax/Bmax
(fmol/(oocyte × sec)) m) (fmol/oocyte) (nm) (sec−1)
66.9 ± 6.3 2.71-b 152.5 ± 7.0 5.21-c 0.47 ± 0.06

Mean values (±SEM) for Vmax andBmax were determined in three experiments using different oocyte batches (not voltage-clamped). In each experiment, parallel pools of oocytes were used for Vmax and for Bmax measurements.

F1-a

DA uptake was measured solely with [3H]DA in one experiment and solely by HPLC-EC in a second experiment. Both methods were used in a third experiment and yielded Vmax values that differed by 7%.

F1-b

CI95 0.2–36 μm.

F1-c

CI95 2.9–9.2 nm.