Bioconjugates are an important class of therapeutic molecules. To date, glycan-based metabolic glycoengineering has had limited use in this field, due to the complexities of the endogenous glycosylation pathway and the lack of an glycosylation consensus sequence. Here, we describe the development of a versatile on-demand glycosylation system that uses a novel, widely applicable 5 amino acid glycosylation tag, and a metabolically engineered UDP-galactose-4-eperimase (GALE) knock-out cell line. Optimization of the primary sequence of the tag enables the production of Fc-based proteins with either single or multiple glycans with complexity fully controlled by media supplementation. We demonstrate how the uniformly labeled proteins containing exclusively N-azido-acetylgalactosamine are used for CLICK chemistry-based bioconjugation to generate site-specifically fluorochrome-labeled antibodies, dual-payload molecules, and bioactive Fc-peptides for applications in basic research and drug discovery. To our knowledge, this is the first description of generating a site-specific glycosylation system by combining an glycosylation tag and a metabolically engineered cell line.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604393PMC
http://dx.doi.org/10.1080/19420862.2021.1992068DOI Listing

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