Abstract
The expression site-associated gene ESAG 6 was previously implicated in transferrin binding in the protozoan parasite Trypanosoma brucei. ESAG 6 and the closely related ESAG 7 of T. brucei strain AnTat1.3 have now been expressed in insect cells using the baculovirus expression system. Expression of ESAG 6 alone in insect cells gives rise to a glycosylated protein of approximately 52 kDa, which is cell surface-associated through a glycosylphosphatidylinositol anchor at its C terminus. The ESAG 7 product of about 42 kDa is also glycosylated, but lacks the glycosylphosphatidylinositol modification, and is located intracellularly. No transferrin-binding activity is observed when either ESAG is expressed independently. However, their expression results in a cell surface complex of ESAG 6 and 7 products that specifically binds transferrin. This shows that both ESAG 6 and 7 products are necessary and sufficient for binding to transferrin.
MeSH Terms
Animals
Carrier Proteins/biosynthesis,genetics,isolation & purification
Cattle
Cell Line
Gene Expression
Genetic Vectors
Glycosylphosphatidylinositols/metabolism
Immunoblotting
Iron-Binding Proteins
Moths
Plasmids
Protozoan Proteins/biosynthesis,genetics,isolation & purification
Recombinant Proteins/biosynthesis,isolation & purification
Restriction Mapping
Transfection
Transferrin-Binding Proteins
Trypanosoma brucei brucei/metabolism
Chemicals
Carrier Proteins
Glycosylphosphatidylinositols
Iron-Binding Proteins
Protozoan Proteins
Recombinant Proteins
Transferrin-Binding Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Chaudhri M
Max-Planck-Institut für Biologie, Abteilung Membranbiochemie, Tübingen, Germany.
Steverding D
Kittelberger D
Tjia S
Overath P
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