N-Glycan Modification of a Recombinant Protein via Coexpression of Human Glycosyltransferases in Silkworm Pupae

• Published in: Scientific reports 2017-05, Vol.7 (1), p.1409-10, Article 1409
• Main Authors: Kato, Tatsuya, Kako, Natsumi, Kikuta, Kotaro, Miyazaki, Takatsugu, Kondo, Sachiko, Yagi, Hirokazu, Kato, Koichi, Park, Enoch Y.
• Format: Article
• Language: English
• Subjects: 38/22; 38/44; 38/77; 631/1647/1511; 631/61/318; 82/80; Actin; Animals; Bombyx; Bombyx mori; Galactose; Gene expression; Genetic Vectors; Glycoproteins; Glycosyltransferases - biosynthesis; Glycosyltransferases - chemistry; Glycosyltransferases - genetics; Humanities and Social Sciences; Humans; Immunoglobulin G; Insect cells; Insects; Mammalian cells; Mammals; Mannose; multidisciplinary; N-Acetylglucosamine; N-Acetylglucosinyldiphosphodolichol N-acetylglucosaminyltransferase; N-glycans; Nucleopolyhedrovirus - genetics; Polyhedrin; Polysaccharides; Polysaccharides - biosynthesis; Polysaccharides - chemistry; Promoter Regions, Genetic; Proteins; Pupa; Pupae; Recombinant Proteins - biosynthesis; Recombinant Proteins - genetics; Science; Science (multidisciplinary)
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-017-01630-6

Recombinant proteins produced in insect cells and insects, unlike those produced in mammalian cells, have pauci-mannose-type N -glycans. In this study, we examined complex-type N -glycans on recombinant proteins via coexpression of human β-1,2- N -acetylglucosaminyltransferase II (hGnT II) and human β1,4-galactosyltransferase (hGalT I) in silkworm pupae, by using the Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid system. The actin A3 promoter from B. mori and the polyhedrin promoter from Autographa californica multiple nucleopolyhedroviruses (AcMNPVs) were used to coexpress hGnT II and hGalT I. These recombinant BmNPVs were coexpressed with human IgG (hIgG), hGnT II and hGalT I in silkworm pupae. When hIgG was coexpressed with hGnT II, approximately 15% of all N -glycans were biantennary, with both arms terminally modified with N -acetylglucosamine (GlcNAc). In contrast, when hIgG was coexpressed with both hGnT II and hGalT I under the control of the polyhedrin promoter, 27% of all N -glycans were biantennary and terminally modified with GlcNAc, with up to 5% carrying one galactose and 11% carrying two. The obtained N -glycan structure was dependent on the promoters used for coexpression of hGnT II or hGalT I. This is the first report of silkworm pupae producing a biantennary, terminally galactosylated N -glycan in a recombinant protein. These results suggest that silkworms can be used as alternatives to insect and mammalian hosts to produce recombinant glycoproteins with complex N -glycans.