Estrogen-binding properties of rat serum α1-fetoprotein and its isoforms. Investigation of the apparent non-integrality of sites on the unfractionated protein

Abstract

Rat fetal serum α₁-fetoprotein (AFP), a heterogeneous glycoprotein, binds estrogens with high affinity but at a fractional number of sites even after treatment with charcoal (n = 0.6), which may mean 60% of the protein has 1 site and the remainder none. To investigate the origin of this fractional number of sites the “native” protein (purified by negative affinity chromatography) was further purified (step 1) and fractionated (step 2) into its two main charge variants (electrophoretically “slow” and “fast”) by a two-step fast-protein liquid chromatography method. The binding parameters for estrone and estradiol-17β of the “native” and “repurified” proteins and of each charge variant were determined by equilibrium microdialysis. The molar extinction coefficient at 278 nm of each sample was also determined. (1) The “repurified” AFP and each charge variant had a number of binding sites for estrogens close to unity. This increase in the number of sites could neither be explained by the loss of a non-binding isoform (corresponding to 40% of the protein) during chromatography, nor by the existence of complex negative modulatory interactions between isoforms.

1. 1.

   (2) The affinities for estrogens of the “repurified” protein and the two charge variants were slightly decreased compared to that of “native” AFP, except that the “fast” form had the “native” protein's high affinity for estrone—but not for estradiol-17β.

2. 2.

   (3) The molar extinction coefficients at 278 nm of the “repurified” AFP and the isoforms were much lower than that of the “native” protein.

These results suggest that the presence of (an) inhibitor(s) of estrogen binding on the “native” protein which is/are removed by the ion-exchange fast protein liquid chromatography (FPLC) column. A ligand absorbing at 278 nm, which may or may not be the inhibitor, is also removed. The isoform heterogeneity with respect to estrone binding is discussed.