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Abstract
Protein glycosylation, the enzymatic modification of amino acid sidechains with sugar moieties, plays critical roles in cellular function, human health, and biotechnology. However, studying and producing defined glycoproteins remains challenging. Cell-free glycoprotein synthesis systems, in which protein synthesis and glycosylation are performed in crude cell extracts, offer new approaches to address these challenges. Here, we review versatile, state-of-the-art systems for biomanufacturing glycoproteins in prokaryotic and eukaryotic cell-free systems with natural and synthetic N-linked glycosylation pathways. We discuss existing challenges and future opportunities in the use of cell-free systems for the design, manufacture, and study of glycoprotein biomedicines.
Details
; Kightlinger Weston 1
; Jewett, Michael C 2
1 Northwestern University, Technological Institute E136, Department of Chemical and Biological Engineering, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, Chemistry of Life Processes Institute, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, Technological Institute E136, Center for Synthetic Biology, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507)
2 Northwestern University, Technological Institute E136, Department of Chemical and Biological Engineering, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, Chemistry of Life Processes Institute, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, Technological Institute E136, Center for Synthetic Biology, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, Robert H. Lurie Comprehensive Cancer Center, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Simpson Querrey Institute, Northwestern University, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507)





