Metabolic Glycoengineering with N‐Acyl Side Chain Modified Mannosamines |
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| Authors: | Paul R Wratil Prof?Dr Rüdiger Horstkorte Prof?Dr Werner Reutter |
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| Affiliation: | 1. Institut für Laboratoriumsmedizin, Klinische Chemie und Pathobiochemie, Charité—Universit?tsmedizin Berlin, Berlin, Germany;2. Institut für Physiologische Chemie, Martin-Luther-Universit?t Halle-Wittenberg, Halle, Germany |
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| Abstract: | In metabolic glycoengineering (MGE), cells or animals are treated with unnatural derivatives of monosaccharides. After entering the cytosol, these sugar analogues are metabolized and subsequently expressed on newly synthesized glycoconjugates. The feasibility of MGE was first discovered for sialylated glycans, by using N‐acyl‐modified mannosamines as precursor molecules for unnatural sialic acids. Prerequisite is the promiscuity of the enzymes of the Roseman–Warren biosynthetic pathway. These enzymes were shown to tolerate specific modifications of the N‐acyl side chain of mannosamine analogues, for example, elongation by one or more methylene groups (aliphatic modifications) or by insertion of reactive groups (bioorthogonal modifications). Unnatural sialic acids are incorporated into glycoconjugates of cells and organs. MGE has intriguing biological consequences for treated cells (aliphatic MGE) and offers the opportunity to visualize the topography and dynamics of sialylated glycans in vitro, ex vivo, and in vivo (bioorthogonal MGE). |
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| Keywords: | glycans metabolic glycoengineering metabolic oligosaccharide engineering N-acetylmannosamine sialic acid |
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