Characterization of the Human Prolyl 4-Hydroxylase Tetramer and its Multifunctional Protein Disulfide-Isomerase Subunit Synthesized in a Baculovirus Expression System

Prolyl 4-hydroxylase (EC 1.14.11.2), an α2β2tetramer, catalyzes the posttranslational formation of 4-hydroxyproline in collagens. The enzyme can easily be dissociated into its subunits, but all attempts to associate a tetramer from the dissociated subunits in vitro have been unsuccessful. Molecular cloning of the catalytically important α subunit has identified two types of cDNA clone due to mutually exclusive alternative splicing. The β subunit is a highly unusual multifunctional polypeptide, being identical to the enzyme protein disulfide-isomerase (EC 5.3.4.1). We report here on expression of the α and β subunits of prolyl 4-hydroxylase and a fully active enzyme tetramer in Spodoptera frugiperda insect cells by baculovirus vectors. When the β subunit was expressed alone, the polypeptide produced was found in a 0.1% Triton X-100 extract of the cell homogenate and was a fully active protein disulfide-isomerase. When either form of the α subunit was expressed alone, only traces of the α subunit could be extracted from the cell homogenate with 0.1% Triton X-100, and 1% SDS was required to obtain efficient solubilization. These α subunits had no prolyl 4-hydroxylase activity. When the cells were coinfected with both α- and β-subunit-producing viruses, an enzyme tetramer was formed, but significant amounts of α and β subunits remained unassociated. The recombinant tetramer was indistinguishable from that isolated from vertebrate tissue in terms of its specific activity and kinetic constants for cosubstrates and the peptide substrate. The two alternatively spliced forms of the α subunit gave enzyme tetramers with identical catalytic properties. Baculovirus expression seems to be an excellent system for mass production of the enzyme tetramer and for detailed investigation of the mechanisms involved in the association of the monomers.