Expression and purification of non-glycosylated Trypanosoma brucei transferrin receptor in insect cells |
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Authors: | Maier Alexander Steverding Dietmar |
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Affiliation: | a Department of Parasitology, Ruprecht-Karls-University, Im Neuenheimer Feld 324, 69120 Heidelberg, Germany b BioMedical Research Centre, School of Medicine, Health Policy and Practice, University of East Anglia, Norwich NR4 7TJ, UK |
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Abstract: | The transferrin receptor of the parasite Trypanosoma brucei is a heterodimeric protein complex encoded by the 2 expression site-associated genes (ESAGs) 6 and 7. ESAG6 is a heterogeneously glycosylated protein of 50-60 kDa modified by a glycosylphosphatidylinositol anchor at the C-terminus, while ESAG7 is a 40-42 kDa glycoprotein carrying an unmodified C-terminus. In order to determine whether glycosylation is necessary for dimer formation and ligand binding, the receptor was expressed in insect cells in the presence of tunicamycin. When insect cells were infected with recombinant ESAG6/ESAG7 double expressor baculovirus and grown in the presence of tunicamycin, non-glycosylated forms of ESAG6 and ESAG7 of 46 and 36 kDa, respectively, were synthesized. The non-glycosylated ESAG6 and ESAG7 were capable of forming a heterodimer and of binding transferrin. This results shows that glycosylation is not necessary for synthesis of a functional T. brucei transferrin receptor. |
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Keywords: | ESAG, expression site-associated gene Glycosylation Insect cells GPI, glycosylphosphatidylinositol PNGase F, N-Glycosidase F Transferrin receptor Trypanosoma brucei Tunicamycin |
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