We describe a new method for producing homogeneous eukaryotic N-glycoproteins. The method involves the engineering and functional transfer of the Campylobacter jejuni glycosylation machinery in Escherichia coli to express glycosylated proteins with the key GlcNAc-Asn linkage. The bacterial glycans were then trimmed and remodeled in vitro by enzymatic transglycosylation to fulfill a eukaryotic N-glycosylation. It provides a potentially general platform for producing eukaryotic N-glycoproteins. © 2010 Nature America, Inc. All rights reserved
From Europe PMC via Jisc Publications RouterHistory: ppub 2021-10-01, epub 2021-10-14Publication sta...
Synthesis of homogenous glycans in quantitative yields represents a major bottleneck to the producti...
N-glycosylation, the enzymatic coupling of oligosaccharides to specific asparagine residues of nasce...
N-linked glycosylation is a common protein post-translational modification where glycans are attache...
Traditionally, glycoproteins have been considered the exclusive property of eukaryotes and archaea, ...
The field of recombinant glycoprotein production in Escherichia coli has advanced with an increase i...
Although Escherichia coli has been engineered to perform N-glycosylation of recombinant proteins, an...
The production of N-linked recombinant glycoproteins is possible in a variety of biotechnology host ...
Abstract Background The production of N-linked glycoproteins in genetically amenable bacterial hosts...
N-linked protein glycosylation is the most abundant posttranslation modification of secretory protei...
<p>A: Standard N-glycosylation pathway in the ER. The early steps in N-glycosylation start with the ...
Here we report a facile and efficient method for site-directed glycosylation of peptide/protein. The...
Escherichia coli is a powerful tool for elucidating many of the basic principles of biology. As a pr...
The experiments contained within this thesis are aimed at improving N-glycoprotein production potent...
The Campylobacter jejuni pgl locus encodes an N-linked protein glycosylation machinery that can be f...
From Europe PMC via Jisc Publications RouterHistory: ppub 2021-10-01, epub 2021-10-14Publication sta...
Synthesis of homogenous glycans in quantitative yields represents a major bottleneck to the producti...
N-glycosylation, the enzymatic coupling of oligosaccharides to specific asparagine residues of nasce...
N-linked glycosylation is a common protein post-translational modification where glycans are attache...
Traditionally, glycoproteins have been considered the exclusive property of eukaryotes and archaea, ...
The field of recombinant glycoprotein production in Escherichia coli has advanced with an increase i...
Although Escherichia coli has been engineered to perform N-glycosylation of recombinant proteins, an...
The production of N-linked recombinant glycoproteins is possible in a variety of biotechnology host ...
Abstract Background The production of N-linked glycoproteins in genetically amenable bacterial hosts...
N-linked protein glycosylation is the most abundant posttranslation modification of secretory protei...
<p>A: Standard N-glycosylation pathway in the ER. The early steps in N-glycosylation start with the ...
Here we report a facile and efficient method for site-directed glycosylation of peptide/protein. The...
Escherichia coli is a powerful tool for elucidating many of the basic principles of biology. As a pr...
The experiments contained within this thesis are aimed at improving N-glycoprotein production potent...
The Campylobacter jejuni pgl locus encodes an N-linked protein glycosylation machinery that can be f...
From Europe PMC via Jisc Publications RouterHistory: ppub 2021-10-01, epub 2021-10-14Publication sta...
Synthesis of homogenous glycans in quantitative yields represents a major bottleneck to the producti...
N-glycosylation, the enzymatic coupling of oligosaccharides to specific asparagine residues of nasce...