BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Abstract
Bilitranslocase (TC 2.A.65.1.1) is an organic anion membrane carrier expressed at the sinusoidal domain of the liver plasma
membrane and in epithelial cells of the gastric mucosa. Its substrates are sulfobromophthalein, bilirubin, and nicotinic acid. This
work reports on the identification of a new class of bilitranslocase substrates, i.e., anthocyanins. Seventeen out these 20 compounds
tested behaved as competitive inhibitors of bilitranslocase transport activity (Ki = 1.4–22 µM). Their structure–activity relationship
reveals that mono- and di-glucosyl anthocyanins, the anthocyanin species occurring in food, are better ligands than the corresponding
aglycones. Moreover, the first interaction of anthocyanins with the carrier occurs through hydrophilic moieties, such as the
3-glucosyl moiety and the Bring for the monoglucosides, through the 5-glucosyl moiety and the A ring for the diglucosides, and
through either the B or the A ring for the aglycones. These findings suggest that bilitranslocase could play a role in the bioavailability
of anthocyanins.