Fig. 1.
Iron transport activity of wild-type and mutant forms of Nramp2. HEK293T cells were transfected with the constructs indicated and uptake of 55Fe (in pmol) was measured. Cells were incubated for 20 minutes in pH 6.0 incubation buffer with 50 μmol/L ascorbate and 1 μmol/L 55Fe-NTA. (−) Indicates iron uptake by cells transfected with an antisense control, in which the murine Nramp2 cDNA was subcloned into pMT2 in a noncoding orientation.