Characterization of a novel GDP-mannose:Serine-protein mannose-l-phosphotransferase from Leishmania mexicana

Protozoan parasites of the genus Leishmania secrete a number of glycoproteins and mucin-like proteoglycans that appear to be important parasite virulence factors. We have previously proposed that the polypeptide backbones of these molecules are extensively modified with a complex array of phosphoglycan chains that are linked to Ser/Thr-rich domains via a common Man alpha 1-PO4-Ser Linkage (Ilg, T., Overath, P., Ferguson, M. A J., Rutherford, T,, Campbell, D, G,, and McConville, M, J, (1994) J, Biol. Chem, 269, 24073-24081), In this study, we show that Leishmania mexicana promastigotes contain a peptide-specific mannose-l-phosphotransferase (pep-MPT) activity that adds Man alpha 1-P to serine residues in a range of defined peptides, The presence and location of the Man alpha 1-PO4-Ser linkage in these peptides were determined by electrospray ionization mass spectrometry and chemical and enzymatic treatments. The pep-MPT activity was solubilized in non-ionic detergents, was dependent on Mn2+, utilized GDP-Man as the mannose donor, and was expressed in all developmental stages of the parasite. The pep-MPT activity was maximal against peptides containing Ser/Thr-rich domains of the endogenous accepters and, based on competition assays with oligosaccharide accepters, was distinct from other leishmanial MPTs involved in the initiation and elongation of lipid-linked phosphoglycan chains. In subcellular fractionation experiments, pep-MPT was resolved from the endoplasmic reticulum marker BiP, but had an overlapping distribution with the cis-Golgi marker Rab1, Although Man-PO4 residues in the mature secreted glycoproteins are extensively modified with mannose oligosaccharides and phosphoglycan chains, similar modifications were not added to peptide-linked Man-PO4 residues in the in vitro assays, Similarly, Man-PO4 residues on endogenous polypeptide accepters were also poorly extended, although the elongating enzymes were still active, suggesting that the pep-MPT activity and elongating enzymes may be present in separate subcellular compartments.