SOYBEAN PROTEIN PRODUCTS AS REGULATORS OF LIVER LOW-DENSITY-LIPOPROTEIN RECEPTORS - I - IDENTIFICATION OF ACTIVE BETA-CONGLYCININ SUBUNITS

The ability of the different soy globulins to upregulate low-density l ipoprotein (LDL) uptake and metabolism in human hepatoma cells (Hep G2 ) was investigated, in an attempt to identify peptide components respo nsible for the upregulation of the LDL receptor. In parallel, the meta bolism of soy globulins, added to the culture medium, was investigated by two-dimensional electrophoresis. After addition of soy globulins, there were no marked changes in the cell protein pattern, as evaluated by general protein staining. By immunodetection, intact 7S components were observed both free in the culture medium and bound to plasma mem branes. Inside cells, alpha + alpha' subunits in their native forms we re not detectable, whereas most of the beta chain was found unchanged. Largely unmodified soybean proteins were detected in a lysate of 11S- treated cells. Incubation of Hep G2 cell with purified alpha + alpha' from 7S sharply increased uptake and degradation of I-125-LDL added to the culture medium, whereas the beta chains were ineffective; 7S itse lf was more active than 11S in this assay. The ability to bring about st specific biological effect such as the observed upregulation of LDL receptors correlates in our test system with the kinetics and/or the extent of catabolism of individual components within the cell.