DIFFERENT MOLECULAR SIZES FOR NA+-DEPENDENT PHOSPHONOFORMIC ACID BINDING AND PHOSPHATE-TRANSPORT IN RENAL BRUSH-BORDER MEMBRANE-VESICLES

We compared several features of Na+-dependent phosphono[14C]formic acid (PFA) binding and Na+-dependent phosphate transport in rat renal brush border membrane vesicles. From kinetic analyses, we estimated an apparent Km for PFA binding of 0.86 mM, an order of magnitude greater than that for phosphate and the high-affinity phosphate transport system. A hyperbolic Na+-saturation curve for PFA binding and a sigmoidal Na+-saturation curve for phosphate transport were demonstrated; based on these data, we estimated stoichiometries of 1:1 for Na+/PFA and 2:1 for Na+/phosphate. By radiation inactivation analysis, target sizes for brush border membrane protein(s) mediating Na+-dependent PFA binding and Na+-dependent phosphate transport corresponded to molecular masses of 555 ± 32 kDa and 205 ± 36 kDa, respectively. Similar analysis of the phosphate-inhibitable component of Na+-dependent PFA binding gave a target size of 130 ± 28 kDa. We also demonstrated that phosphate deprivation, which elicits a 2.6-fold increase in brush border membrane Na+-dependent phosphate transport, had no effect on either Na+-dependent PFA binding or on the target size for PFA binding. However, phosphate deprivation appeared to increase the target size for phosphate transport (from 255 ± 32 to 335 ± 75 kDa (P<0.01)). In summary, we present evidence for several differences between Na+-dependent PFA binding and Na+-dependent phosphate transport in rat renal brush border membrane vesicles and suggest that PFA may not interact exclusively with the proteins mediating Na+-phosphate co-transport. © 1990.