Litcius/Paper detail

Application of the Inverse-Electron-Demand Diels-Alder Reaction for Metabolic Glycoengineering

Lisa Maria Haiber, Markus Kufleitner, Valentin Wittmann

2021Frontiers in Chemistry27 citationsDOIOpen Access PDF

Abstract

) reaction is an emerging bioorthogonal ligation reaction that finds application in all areas of chemistry and chemical biology. In this review we highlight its application in metabolic glycoengineering (MGE). MGE is a versatile tool to introduce unnatural sugar derivatives that are modified with a chemical reporter group into cellular glycans. The IEDDA reaction can then be used to modify the chemical reporter group allowing, for instance, the visualization or isolation of glycoconjugates. During the last years, many different sugar derivatives as well as reporter groups have been published. These probes are summarized, and their chemical and biological properties are discussed. Furthermore, we discuss examples of MGE and subsequent IEDDA reaction that highlight its suitability for application within living systems.

Topics & Concepts

Bioorthogonal chemistryGlycoconjugateGlycanClick chemistryChemistryCombinatorial chemistryBiochemistryChemical biologyChemical reactionGlycoproteinClick Chemistry and ApplicationsChemical Synthesis and AnalysisCarbohydrate Chemistry and Synthesis
Application of the Inverse-Electron-Demand Diels-Alder Reaction for Metabolic Glycoengineering | Litcius