In a previous paper, the biological activity of a 216-amino acid recombinant truncated form of the soybean 7S globulin alpha' subunit, known to control cholesterol and triglyceride homeostasis, was described. In this work, a shorter version of the polypeptide chain, spanning 142 amino acid residues from the N-terminus and thus exclusively including the so-called extension region, was cloned and overexpressed in Pichia pastoris. The yield of the recombinant polypeptide, which was termed alpha'E. was 8-fold greater than the previous truncated version. The alpha'E polypeptide was purified by simple conventional biochemical techniques to make it available for biological assays. Human hepatoma cell lines (Hep G2) were used to monitor the uptake and degradation of labeled low-density lipoproteins (LDL), according to an established procedure. The LDL uptake (+86%) and degradation (+94%) by cells tested at the highest alpha'E dose (2 mu M) were similar to those found in cells incubated with 1 mu M simvastatin, a potent inhibitor of cholesterol biosynthesis. Additionally, the cell response to alpha'E was found to be dose-dependent. The present findings strongly suggest that this recombinant polypeptide, or a fragment thereof, is the molecular determinant for cholesterol homeostasis and open new prospects for understanding the mechanism involved in this biological response, as a gateway to its utilization in lipid-lowering therapies. (C) 2011 Elsevier Inc. All rights reserved.