Functional characterization of albumin binding to the apical membrane of OK cells

M Gekle, S Mildenberger… - American Journal of …, 1996 - journals.physiology.org
M Gekle, S Mildenberger, R Freudinger, S Silbernagl
American Journal of Physiology-Renal Physiology, 1996journals.physiology.org
We characterized binding of albumin to the apical membrane of opossum kidney (OK) cells
using fluorescein isothiocyanate (FITC)-albumin (ie, bovine serum albumin, BSA) as
substrate. Functional analysis of binding data showed one specific binding site
characterized by half-maximal binding (Michaelis constant,(Km) at 20 mg/l (300 nmol/l) and
maximal binding capacity (Bmax) of 0.61 microgram/mg cellular protein. Excess of
unlabeled albumin (BSA) inhibited binding at low concentrations of FITC-albumin …
We characterized binding of albumin to the apical membrane of opossum kidney (OK) cells using fluorescein isothiocyanate (FITC)-albumin (i.e., bovine serum albumin, BSA) as substrate. Functional analysis of binding data showed one specific binding site characterized by half-maximal binding (Michaelis constant, (Km) at 20 mg/l (300 nmol/l) and maximal binding capacity (Bmax) of 0.61 microgram/mg cellular protein. Excess of unlabeled albumin (BSA) inhibited binding at low concentrations of FITC-albumin completely but only partially at high concentrations. FITC-albumin binding was reversible and pH dependent. Km increased about sixfold when pH decreased from 7.4 to 5.0. The inhibitory effects of conalbumin, alpha-lactalbumin, and transferrin were significantly smaller compared with BSA. We conclude that OK cells express a high-affinity binding site for albumin on the apical membrane. This binding site is pH sensitive, binds albumin in the physiological range, and could be responsible for the effective receptor-mediated reabsorption of albumin in the proximal tubule.
American Physiological Society