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. 2010 Oct 27;300(1):C14–C21. doi: 10.1152/ajpcell.00388.2010

Table 1.

Comparison of kinetic and thermodynamic properties of hSGLT2 and hSGLT1 at 37°C

hSGLT2 hSGLT1
K0.5d-glucose, mM 4.9 ± 0.6 1.8 ± 0.2
K0.5αMDG, mM 6.0 ± 0.9 3.8 ± 0.2
K0.5d-galactose, mM ≥100 6.1 ± 0.4
K0.5Na, mM 25 ± 10 73 ± 19
Hill coefficient (nh) 0.9 ± 0.2 1.5 ± 0.1
Na+:glucose coupling (n) 1:1 2:1
Kiphlorizin, nM 11 ± 0.9 140 ± 15
t1/2,Offphlorizin, s 24 ± 3 4 ± 0.5
kOffphlorizin, s−1 0.030 ± 0.003 0.19 ± 0.02
kOnphlorizin, M/s 2.7 × 106 1.4 × 106

Values are means ± SE for n ≥ 3 cells at −60 mV. Rate constant for phlorizin binding (kOnphlorizin) is calculated from the Ki and the phlorizin release rate constant (kOffphlorizin). hSGLT, human Na+/d-glucose cotransporter; αMDG, [14C]-α-methyl-d-glucopyranoside; K0.5, substrate concentration at half-maximal current; t1/2,Off, half-time of recovery of glucose current after removal of phlorizin.