Figure 7.
Figure 7. Comparative assessment of the transport properties of WT and Nramp2G185R. (A) Measurements of calcein fluorescence in cells expressing WT Nramp2 or Nramp2G185R. Cells were initially bathed at pH 7.3 and pH was lowered to 5.5 where indicated. Finally, 100 μMCo2+ or Fe2+ was added as noted. Representative raw data are illustrated. (B) Co2+ uptake determinations by cells transfected with WT or Nramp2G185R, calculated from experiments like that in panel A. Data are presented as the ratio of the initial fluorescence (F0) divided by the fluorescence (F) recorded at the indicated times. (C) The initial rates of Co2+ transport, measured as in panel B, were normalized by the number of surface-exposed Nramp2 molecules, determined in parallel with anti-HA antibodies, as described in “Materials and methods.” To facilitate comparison, the specific transport activity of the mutants is expressed as a fraction of the WT. Data are means plus or minus SE of 6 individual determinations. * P < .05, determined by Student t test. (D) Eadie-Hofstee plot of the transport activity of WT (▪) and Nramp2G185R (○) as a function of the concentration of Co2+. Data are means plus or minus SE of 6 determinations. (E) pH dependence of Co2+ transport in cells transfected with WT or Nramp2G185R. Measurements of the specific transport activity are presented as a fraction of the activity of WT Nramp2 at pH 5.5. Data are means plus or minus SE of 4 determinations.

Comparative assessment of the transport properties of WT and Nramp2G185R. (A) Measurements of calcein fluorescence in cells expressing WT Nramp2 or Nramp2G185R. Cells were initially bathed at pH 7.3 and pH was lowered to 5.5 where indicated. Finally, 100 μMCo2+ or Fe2+ was added as noted. Representative raw data are illustrated. (B) Co2+ uptake determinations by cells transfected with WT or Nramp2G185R, calculated from experiments like that in panel A. Data are presented as the ratio of the initial fluorescence (F0) divided by the fluorescence (F) recorded at the indicated times. (C) The initial rates of Co2+ transport, measured as in panel B, were normalized by the number of surface-exposed Nramp2 molecules, determined in parallel with anti-HA antibodies, as described in “Materials and methods.” To facilitate comparison, the specific transport activity of the mutants is expressed as a fraction of the WT. Data are means plus or minus SE of 6 individual determinations. *P < .05, determined by Student t test. (D) Eadie-Hofstee plot of the transport activity of WT (▪) and Nramp2G185R (○) as a function of the concentration of Co2+. Data are means plus or minus SE of 6 determinations. (E) pH dependence of Co2+ transport in cells transfected with WT or Nramp2G185R. Measurements of the specific transport activity are presented as a fraction of the activity of WT Nramp2 at pH 5.5. Data are means plus or minus SE of 4 determinations.

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