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Humanization of Yeast to Produce Complex Terminally Sialylated Glycoproteins

Stephen R. Hamilton, Robert C. Davidson, Natarajan Sethuraman, Juergen H. Nett, Youwei Jiang, Sandra E. Rios, Piotr Bobrowicz, Terrance A. Stadheim, Huijuan Li, Byung-Kwon Choi, Daniel C. Hopkins, Harry Wischnewski, Jessica Roser, Teresa Mitchell, Rendall R. Strawbridge, Jack P. Hoopes, Stefan Wildt, Tillman U. Gerngross

📄 Abstract

Yeast is a widely used recombinant protein expression system. We expanded its utility by engineering the yeast Pichia pastoris to secrete human glycoproteins with fully complex terminally sialylated N-glycans. After the knockout of four genes to eliminate yeast-specific glycosylation, we introduced 14 heterologous genes, allowing us to replicate the sequential steps of human glycosylation. The reported cell lines produce complex glycoproteins with greater than 90% terminal sialylation. Finally, to demonstrate the utility of these yeast strains, functional recombinant erythropoietin was produced.

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