CHAPTER 6: Chemoenzymatic Synthesis of N-Glycans
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Published:20 Mar 2017
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Special Collection: 2017 ebook collectionSeries: Chemical Biology
X. Cao, J. Zhou, Y. Guo, Y. Liu, L. Li, and P. G. Wang, in Chemical Biology of Glycoproteins, ed. Z. Tan and L. Wang, The Royal Society of Chemistry, 2017, pp. 188-208.
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A major post-translational modification of proteins on cell surfaces is asparagine N-linked glycosylation, which plays critical roles in various biological processes. Over the past decade, efficient strategies for the synthesis of N-glycans have become increasingly attractive because it is highly desired to obtain structurally defined N-glycans in sufficient amounts for structure–function studies. In this respect, chemical synthesis of N-glycans has been well developed and has become the most frequently used approach to generate well-defined N-glycans. However, when synthetic targets are complicated N-glycans and especially N-glycan libraries, the chemical approach still remains challenging, tedious, and time-consuming. More recently, a facile and practical strategy, core synthesis/enzymatic extension (CSEE), has been developed for efficient synthesis of N-glycan libraries with structural diversities, wherein an N-glycan core is first chemically synthesized and further elongated by glycosyltransferases (GTs) to rapidly produce a large number of complex N-glycans. Herein, we provide a concise summary of most recent advances in chemical and chemoenzymatic synthesis of N-glycans.